Inhibitors of ret

ABSTRACT

Described herein are compounds that inhibit wild-type RET and its resistant mutants, pharmaceutical compositions including such compounds, and methods of using such compounds and compositions.

CLAIM OF PRIORITY

This application is a continuation of U.S. application Ser. No.15/340,428, filed Nov. 1, 2016, which claims priority from U.S.Provisional Application No. 62/249,784, filed Nov. 2, 2105, and U.S.Provisional Application No. 62/367,960, filed Jul. 28, 2016, each ofwhich is incorporated herein by reference in its entirety.

This invention relates to inhibitors of RET that are active againstwild-type RET and its resistant mutants.

BACKGROUND

RET (rearranged during transfection) is a receptor tyrosine kinase thatactivates multiple downstream pathways involved in cell proliferationand survival. RET fusions are implicated in several cancers includingpapillary thyroid carcinoma and non-small cell lung cancer. A genomicsanalysis on the landscape of kinase fusions identified RET fusions inbreast and colon cancer patient samples, providing therapeutic rationalefor the use of RET inhibitors in multiple patient subpopulations.

The identification of RET fusions as drivers in some cancers promptedthe use of approved multi-kinase inhibitors with RET inhibitory activityto treat patients whose tumors express a RET fusion protein. However,these drugs cannot always be dosed at the levels required tosufficiently inhibit RET due to toxicities that result from inhibitionof targets other than RET. Further, one of the greatest challenges intreating cancer is the ability of tumor cells to become resistant totherapy. Kinase reactivation via mutation is a common mechanism ofresistance. When resistance occurs, the patient's treatment options areoften very limited, and the cancer progresses, unchecked, in mostinstances. There is thus a need for compounds that inhibit RET, as wellas its resistant mutants.

SUMMARY

The present invention provides inhibitors of RET and RET mutants, e.g.,RET resistant mutants (as defined herein), for example, inhibitors ofstructural formula (I) and pharmaceutically acceptable salts andcompositions thereof. The present invention further provides methods ofusing the compounds of the invention, and pharmaceutically acceptablesalts and compositions thereof, to inhibit the activity of RET or RETmutants in a cell or patient. The present invention still furtherprovides methods for using the compounds of the invention, andpharmaceutically acceptable salts and compositions thereof, to treat asubject suffering from a condition mediated by aberrant RET activity,e.g., cancer.

In one aspect, the invention features a compound of structural formula(A) or a pharmaceutically acceptable salt thereof:

wherein each of ring A, X¹, X², Y¹, Y², R¹, R², R^(3a), R^(3b), R⁴, R⁵,R⁶, R⁷, R^(8a), R^(8b), R⁹, m, n, o and

“

” is defined as described herein.

In another aspect, the present invention provides pharmaceuticalcompositions comprising a compound of structural formula (I) or apharmaceutically acceptable salt thereof and a pharmaceuticallyacceptable carrier.

In another aspect, the present invention provides a method forinhibiting RET activity in a cell or in a patient. In some embodiments,said method comprises the step of contacting the cell or administeringto the patient a compound of structural formula (I) or apharmaceutically acceptable salt or composition thereof.

In another aspect, the present invention provides a method for treatinga subject suffering from a condition mediated by aberrant RET activity.In some embodiments, said method comprises administering to the subjecta therapeutically effective amount of a compound of structural formula(I) or a pharmaceutically acceptable salt or composition thereof.

In another aspect, the present invention provides a method for treatinga subject who has developed resistance to a cancer treatment. In someembodiments, said method comprises administering to the subject atherapeutically effective amount of a compound of structural formula (I)or a pharmaceutically acceptable salt or composition thereof.

EMBODIMENTS OF THE INVENTION Compounds

In one aspect, the present invention features a compound having thestructural formula (A):

or a pharmaceutically acceptable salt thereof, wherein:

ring A is an aryl or heteroaryl ring;

each of X¹ and X² is independently selected from N and C(R⁶);

each of Y¹ and Y² is independently selected from —CH₂— and —O—, whereinno more than one of Y¹ or Y² is —O—;

each R¹ and each R⁷ is independently selected from selected from C₁-C₆alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, halo, C₁-C₆heteroalkyl, cycloalkyl, aryl, heteroaryl, aryloxy, aralkyl,heterocyclyl, heterocyclylalkyl, nitro, cyano, —C(O)R, —OC(O)R, —C(O)OR,—(C₁-C₆ alkylene)-C(O)R, —SR, —S(O)₂R, —S(O)₂—N(R)(R), —(C₁-C₆alkylene)-S(O)₂R, —(C₁-C₆ alkylene)-S(O)₂—N(R)(R), —N(R)(R),—C(O)—N(R)(R), —N(R)—C(O)R, —N(R)—C(O)OR, —(C₁-C₆ alkylene)-N(R)—C(O)R,—N(R)S(O)₂R, and —P(O)(R)(R); wherein each of alkyl, alkenyl, alkynyl,alkoxy, heteroalkyl, cycloalkyl, aryl, heteroaryl, aryloxy, aralkyl,heterocyclyl, and heterocyclylalkyl is independently substituted with0-5 occurrences of R^(a); or two R¹ or two R⁷ are taken together withthe carbon atoms to which they are attached form a cycloalkyl orheterocyclyl ring independently substituted with 0-5 occurrences ofR^(b);

each of R² when present, R^(3a), R^(3b), R⁴, R^(8a) and R^(8b), whenpresent is independently selected from hydrogen, C₁-C₆ alkyl, C₁-C₆alkoxy, halo, hydroxyl, C₁-C₆ heteroalkyl, and —N(R)(R); wherein eachalkyl, alkoxy, and heteroalkyl is optionally and independentlysubstituted with 0-5 occurrences of R^(a);

each of R⁵ and R⁹ is independently selected from hydrogen, C₁-C₆ alkyl,and C₁-C₆ heteroalkyl; wherein each alkyl and heteroalkyl is optionallyand independently substituted with 0-5 occurrences of R^(a);

each R⁶ is independently selected from hydrogen, C₁-C₆ alkyl, C₁-C₆alkoxy, halo, C₁-C₆ heteroalkyl, and —N(R)(R); wherein each alkyl,alkoxy, and heteroalkyl is optionally and independently substituted with0-5 occurrences of R^(a);

each R is independently selected from hydrogen, hydroxyl, halo, thiol,C₁-C₆ alkyl, C₁-C₆ thioalkyl, C₁-C₆ alkoxy, C₁-C₆ heteroalkyl,cycloalkyl, cycloalkylalkyl, heteroarylalkyl, heterocyclyl, andheterocyclylalkyl, wherein each of alkyl, thioalkyl, alkoxy,heteroalkyl, cycloalkyl, cycloalkylalkyl, heteroarylalkyl, heterocyclyl,and heterocyclylalkyl is independently substituted with 0-5 occurrencesof R^(a), or 2 R¹ together with the atom(s) to which they are attachedform a cycloalkyl or heterocyclyl ring independently substituted with0-5 occurrences of R^(b);

each R^(a) and each R^(b) is independently selected from C₁-C₆ alkyl,halo, hydroxyl, C₁-C₆ heteroalkyl, C₁-C₆ alkoxy, cycloalkyl,heterocyclyl, or cyano, wherein each of alkyl, heteroalkyl, alkoxy,cycloalkyl and heterocyclyl is independently substituted with 0-5occurrences of R′;

each R′ is independently selected from C₁-C₆ alkyl, C₁-C₆ heteroalkyl,halo, hydroxyl, cycloalkyl or cyano; or 2 R′ together with the atom(s)to which they are attached form a cycloalkyl or heterocyclyl ring;

m is 0, 1, or 2;

n is 0, 1, 2, or 3;

represents a single or double bond;

each o is 0 when

is a double bond; and

each o is 1 when

is a single bond.

In some embodiments, the compound is a compound having formula (I):

or a pharmaceutically acceptable salt thereof, wherein each of ring A,X¹, X², R¹, R², R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R^(8b), R⁹, R,R^(a), R^(b), R′, m, and n is as described for a compound of Formula A.

In some embodiments,

represents a single bond and the compound has formula Ia:

or a pharmaceutically acceptable salt thereof, wherein each of ring A,X¹, X², R¹, R², R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R^(8b), R⁹, R,R^(a), R^(b), R′, m, and n is as described for a compound of Formula A.

In some embodiments,

represents a double bond and the compound has formula Ib:

or a pharmaceutically acceptable salt thereof, wherein each of ring A,X¹, X², R¹, R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R⁹, R, R^(a), R^(b),R′, m, and n is as described for a compound of Formula A.

In some embodiments of any of Formulae A, I, Ia or Ib, R¹ is located atthe 5-position. In some embodiments, R¹ is located at the 4-position. Insome embodiments, R¹ is C₁-C₄ alkyl optionally substituted with 0-3occurrences of R^(a). In some embodiments, m is 1 or 2. In someembodiments, m is 1. In some embodiments, m is 1; R¹ is located at the5-position; and R¹ is C₁-C₄ alkyl optionally substituted with 0-3occurrences of R^(a). In some embodiments, R¹ is —CH₃.

In some embodiments of Formulae T or Ia, R² is selected from hydrogen,hydroxyl, halo and O—C₁-C₄ alkyl. In some embodiments, R² is selectedfrom hydrogen, hydroxyl, fluoro and —OCH₃.

In some embodiments any of Formulae A, I, Ia or Ib, each of R^(3a),R^(3b), R^(8a) and R^(8b) (which is only present in Formulae I or Ia) isindependently selected from hydrogen and C₁-C₄ alkyl optionallysubstituted with 0-3 occurrences of R^(a). In some embodiments, each ofR^(3a), R^(3b), R^(8a) and R^(8b) is independently selected fromhydrogen and —CH₃. In some embodiments, at least one pair of R^(3a) andR^(3b) or R^(8a) and R^(8b) is simultaneously hydrogen.

In some embodiments any of Formulae A, I, Ia or Ib, R⁴ is selected fromhydrogen, C₁-C₄ alkyl, and O—C₁-C₄ alkyl, wherein each alkyl portion ofR⁴ is optionally substituted with 0-3 occurrences of R^(a). In someembodiments, R⁴ is selected from hydrogen, —CH₃, —CH₂CH₃, —OCH₃ and—OCH₂CH₃.

In some embodiments any of Formulae A, I, Ia or Ib, R⁵ is selected fromhydrogen and C₁-C₄ alkyl optionally substituted with 0-3 occurrences ofR^(a). In some embodiments, R⁵ is selected from hydrogen and —CH₃.

In some embodiments any of Formulae A, I, Ia or Ib, each R⁶ isindependently selected from hydrogen, halo, and C₁-C₄ alkyl optionallysubstituted with 0-3 occurrences of R^(a). In some embodiments, each R⁶is independently selected from hydrogen, chloro, and —CH₃. In someembodiments, no more than one R⁶ is other than hydrogen.

In some embodiments any of Formulae A, I, Ia or Ib, ring A is a6-membered monocyclic heteroaryl comprising at least one nitrogen ringatom. In some embodiments, ring A is selected from

In some embodiments any of Formulae A, I, Ia or Ib, R⁷ is heteroaryloptionally substituted with 0-3 occurrences of R^(b). In someembodiments, R⁷ is selected from 4-fluoropyrazole-1-yl,4-chloropyrazol-1-yl, pyrazol-1-yl, and 3,5-dimethylpyrazol-1-yloptionally substituted with 0-3 occurrences of R^(b). In someembodiments, R⁷ is pyrazol-1-yl optionally substituted with 0-3occurrences of R^(b). In some embodiments, n is 1. In some embodiments,n is 1; and R⁷ is pyrazol-1-yl an optionally substituted with 0-3occurrences of R^(b).

In some embodiments any of Formulae A, I, Ia or Ib, R⁹ is selected fromhydrogen and C₁-C₄ alkyl optionally substituted with 0-3 occurrences ofR^(a). In some embodiments, R⁹ is hydrogen. In some embodiments, R⁹ isC₁-C₄ alkyl. In some embodiments, R⁵ and R⁹ are both hydrogen.

In some embodiments, the compound is a compound having the structuralformula (Ic):

or a pharmaceutically acceptable salt thereof,wherein ring A, X¹, X², R¹, R², R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a),R^(8b), R⁹, m and n are as defined for Formula (A).

In some embodiments, the compound is a compound having the structuralformula (Id):

or a pharmaceutically acceptable salt thereof,wherein ring A, X¹, X², R¹, R², R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a),R^(8b), R⁹, m and n are as defined for Formula (A).

In some embodiments, the compound is a compound having the structuralformula Ie:

or a pharmaceutically acceptable salt thereof,wherein ring A, X¹, X², R¹, R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R⁹,m and n are as defined for Formula (A).

In some embodiments, the compound is a compound having the structuralformula (If):

or a pharmaceutically acceptable salt thereof,wherein ring A, X¹, X², R¹, R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R⁹,m and n are as defined for Formula (A).In another aspect, the present invention features a compound having thestructural formula (II):

or a pharmaceutically acceptable salt thereof, wherein:

X¹ is selected from N, CH and C(halo);

X² is selected from N and CH;

X³ is selected from N and CH;

R¹² is selected from hydrogen, hydroxyl, halo and O—C₁-C₄ alkyl;

each of R^(13a), R^(13b), R^(18a) and R^(18b) is independently selectedfrom hydrogen and C₁-C₄ alkyl;

R¹⁴ is selected from hydrogen, —C₁-C₄ alkyl and —O—C₁-C₄ alkyl;

R¹⁵ is selected from hydrogen and —C₁-C₄ alkyl;

R¹⁶ is selected from hydrogen and —C₁-C₄ alkyl;

R^(17b) is selected from hydrogen and halo; and

R^(17b) and R^(17c) are independently selected from hydrogen and —C₁-C₄alkyl.

In some embodiments, X¹ is selected from N, CH and C(Cl); X² is selectedfrom N and CH; X³ is selected from N and CH; R¹² is selected fromhydrogen, hydroxyl, fluoro and —O—CH₃; each of R^(13a), R^(13b), R^(18a)and R^(18b) is independently selected from hydrogen, methyl and ethyl;and wherein at least one pair of R^(13a) and R^(13b) or R^(18a) andR^(18b) is simultaneously hydrogen; R¹⁴ is selected from hydrogen, —CH₃,—CH₂CH₃, —OCH₃ and —OCH₂CH₃; R¹⁵ is selected from hydrogen and —CH₃; R¹⁶is selected from hydrogen and —CH₃; R^(17b) is selected from hydrogen,chloro and fluoro; R^(17a) and R^(17c) are simultaneously hydrogen or—CH₃, wherein when R^(17a) and R^(17c) are simultaneously —CH₃, R^(17b)is hydrogen.

In some embodiments, the compound is a compound having the structuralformula (IIa):

or a pharmaceutically acceptable salt thereof,wherein X¹, X², X³, R¹², R^(13a), R^(13b), R¹⁴, R¹⁵, R¹⁶, R^(17a),R^(17b), R^(17c), R^(18a), and R^(18b) are as defined as for Formula(II).

In some embodiments, the compound is a compound having the structuralformula (IIb):

or a pharmaceutically acceptable salt thereof,wherein X¹, X², X³, R¹², R^(13a), R^(13b), R¹⁴, R¹⁵, R¹⁶, R^(17a),R^(17b), R^(17c), R^(18a), and R^(18b) are as defined as for Formula(II).

In some embodiments, the invention provides a compound of Formula IIIcor Formula IIIb:

or a pharmaceutically acceptable salt thereof, wherein each of ring A,X¹, X², R¹, R², R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R^(8b), R⁹, R,R^(a), R^(b), R′, m, and n is as described for a compound of Formula A,including the more specific embodiments and aspects of each of the abovevariables.

In some embodiments of Formula IIIb, the compound has the FormulaIIIb-1:

or a pharmaceutically acceptable salt thereof, wherein each of ring A,X¹, X², R¹, R², R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R^(8b), R⁹, R,R^(a), R^(b), R′, m, and n is as described for a compound of Formula A,including the more specific embodiments and aspects of each of the abovevariables.

In some embodiments of Formula IIIb, the compound has the FormulaIIIb-2:

or a pharmaceutically acceptable salt thereof, wherein each of ring A,X¹, X², R¹, R², R^(3a), R^(3b), R⁴, R⁵, R⁶, R⁷, R^(8a), R⁹, R, R^(a),R^(b), R′, m, and n is as described for a compound of Formula A,including the more specific embodiments and aspects of each of the abovevariables.

In some embodiments of Formulae IIIa, IIIb, IIIb-1 and IIIb-2, each ofX¹ and X² is C(R⁶). In one aspect of these embodiments, each of X¹ andX² is CH.

In some embodiments of Formula IIIb, the compound has the Formula IIIb-3or IIIb-4:

or a pharmaceutically acceptable salt thereof, wherein each of R¹²,R^(13a), R^(13b), R¹⁴, R¹⁵, R¹⁶, R^(17a), R^(17b), R^(17c), R^(18a) andR^(18b) are as defined for Formula II, including the more specificembodiments and aspects of each of the above variables.

In some embodiments, the present invention features a compound selectedfrom any compound in Table 1.

In another aspect, the present invention features a pharmaceuticalcomposition comprising a compound of Formula A, I, Ia, lb, Ic, Id, II,IIa, IIb, IIIa, IIIb, IIIb-1, IIIb-2, IIIb-3, or IIIb-4 described herein(e.g., a compound in Table 1) or a pharmaceutically acceptable saltthereof, and a pharmaceutically acceptable carrier.

In another aspect, the present invention features a method forinhibiting RET activity in a cell or in a patient comprising the step ofcontacting the cell or administering to the patient a compound describedherein (e.g., a compound in Table 1) or a pharmaceutically acceptablesalt thereof, or a pharmaceutical composition thereof.

In another aspect, the present invention features a method for treatinga subject suffering from a condition mediated by aberrant RET activity,comprising administering to the subject a therapeutically effectiveamount of a compound described herein (e.g., a compound in Table 1) or apharmaceutically acceptable salt thereof, or a pharmaceuticalcomposition thereof.

In another aspect, the present invention features a method for treatinga subject who has developed resistance to a cancer treatment, comprisingadministering to the subject a therapeutically effective amount of acompound described herein (e.g., a compound in Table 1) or apharmaceutically acceptable salt thereof, or a pharmaceuticalcomposition thereof.

Definitions

As used herein, the terms a “patient,” “subject,” “individual,” and“host” refer to either a human or a non-human animal suffering from orsuspected of suffering from a disease or disorder associated withaberrant RET expression (i.e., increased RET activity caused bysignaling through RET) or biological activity.

“Treat” and “treating” such a disease or disorder refers to amelioratingat least one symptom of the disease or disorder. These terms, when usedin connection with a condition such as a cancer, refer to one or moreof: impeding growth of the cancer, causing the cancer to shrink byweight or volume, extending the expected survival time of the patient,inhibiting tumor growth, reducing tumor mass, reducing size or number ofmetastatic lesions, inhibiting the development of new metastaticlesions, prolonging survival, prolonging progression-free survival,prolonging time to progression, and/or enhancing quality of life.

The term “therapeutic effect” refers to a beneficial local or systemiceffect in animals, particularly mammals, and more particularly humans,caused by administration of a compound or composition of the invention.The phrase “therapeutically-effective amount” means that amount of acompound or composition of the invention that is effective to treat adisease or condition caused by over expression of RET or aberrant RETbiological activity at a reasonable benefit/risk ratio. Thetherapeutically effective amount of such substance will vary dependingupon the subject and disease condition being treated, the weight and ageof the subject, the severity of the disease condition, the manner ofadministration and the like, which can readily be determined by one ofskill in the art.

As used herein, “developing resistance” means that when a drug is firstadministered to the patient, the patient's symptoms improve, whethermeasured by decrease in tumor volume, a decrease in the number of newlesions, or some other means that a physician uses to judge diseaseprogression; however, those symptoms stop improving, or even worsen atsome point. At that time, the patient is said to have developedresistance to the drug.

“Aliphatic group” means a straight-chain, branched-chain, or cyclichydrocarbon group and includes saturated and unsaturated groups, such asan alkyl group, an alkenyl group, and an alkynyl group.

“Alkylene” refers to a divalent radical of an alkyl group, e.g., —CH₂—,—CH₂CH₂—, and —CH₂CH₂CH₂—.

“Alkenyl” means an aliphatic group containing at least one double bond.

“Alkoxyl” or “alkoxy” means an alkyl group having an oxygen radicalattached thereto. Representative alkoxyl groups include methoxy, ethoxy,propyloxy, tert-butoxy and the like. The term “haloalkoxy” refers to analkoxy in which one or more hydrogen atoms are replaced by halo, andincludes alkoxy moieties in which all hydrogens have been replaced byhalo (e.g., perfluoroalkoxy).

“Alkyl” refers to a monovalent radical of a saturated straight orbranched hydrocarbon, such as a straight or branched group of 1-12,1-10, or 1-6 carbon atoms, referred to herein as C₁-C₁₂ alkyl, C₁-C₁₀alkyl, and C₁-C₆ alkyl, respectively. Exemplary alkyl groups include,but are not limited to, methyl, ethyl, propyl, isopropyl,2-methyl-1-propyl, 2-methyl-2-propyl, 2-methyl-1-butyl,3-methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl,2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl,2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl,2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, butyl,isobutyl, t-butyl, pentyl, isopentyl, neopentyl, hexyl, heptyl, octyl,etc.

“Alkenylene” refers to an alkenyl group having two connecting points.For example, “ethenylene” represents the group —CH═CH—. Alkenylenegroups can also be in an unsubstituted form or substituted form with oneor more substituents.

“Alkynyl” refers to a straight or branched hydrocarbon chain containing2-12 carbon atoms and characterized in having one or more triple bonds.Examples of alkynyl groups include, but are not limited to, ethynyl,propargyl, and 3-hexynyl. One of the triple bond carbons may optionallybe the point of attachment of the alkynyl substituent.

“Alkynylene” refers to an alkynyl having two connecting points. Forexample, “ethynylene” represents the group —C≡C—. Alkynylene groups canalso be in an unsubstituted form or substituted form with one or moresubstituents.

“Aromatic ring system” is art-recognized and refers to a monocyclic,bicyclic or polycyclic hydrocarbon ring system, wherein at least onering is aromatic.

“Aryl” refers to a monovalent radical of an aromatic ring system.Representative aryl groups include fully aromatic ring systems, such asphenyl, naphthyl, and anthracenyl, and ring systems where an aromaticcarbon ring is fused to one or more non-aromatic carbon rings, such asindanyl, phthalimidyl, naphthimidyl, or tetrahydronaphthyl, and thelike.

“Arylalkyl” or “aralkyl” refers to an alkyl moiety in which an alkylhydrogen atom is replaced by an aryl group. Aralkyl includes groups inwhich more than one hydrogen atom has been replaced by an aryl group.Examples of “arylalkyl” or “aralkyl” include benzyl, 2-phenylethyl,3-phenylpropyl, 9-fluorenyl, benzhydryl, and trityl groups.

“Aryloxy” refers to —O-(aryl), wherein the heteroaryl moiety is asdefined herein.

“Halo” refers to a radical of any halogen, e.g., —F, —Cl, —Br, or —I.

“Heteroalkyl” refers to an optionally substituted alkyl, which has oneor more skeletal chain atoms selected from an atom other than carbon,e.g., oxygen, nitrogen, sulfur, phosphorus or combinations thereof. Anumerical range may be given, e.g. C₁-C₆ heteroalkyl which refers to thenumber of carbons in the chain, which in this example includes 1 to 6carbon atoms. For example, a —CH₂OCH₂CH₃ radical is referred to as a“C₃” heteroalkyl. Connection to the rest of the molecule may be througheither a heteroatom or a carbon in the heteroalkyl chain.“Heteroalkylene” refers to a divalent optionally substituted alkyl,which has one or more skeletal chain atoms selected from an atom otherthan carbon, e.g., oxygen, nitrogen, sulfur, phosphorus or combinationsthereof.

“Carbocyclic ring system” refers to a monocyclic, bicyclic or polycyclichydrocarbon ring system, wherein each ring is either completelysaturated or contains one or more units of unsaturation, but where noring is aromatic.

“Carbocyclyl” refers to a monovalent radical of a carbocyclic ringsystem. Representative carbocyclyl groups include cycloalkyl groups(e.g., cyclopentyl, cyclobutyl, cyclopentyl, cyclohexyl and the like),and cycloalkenyl groups (e.g., cyclopentenyl, cyclohexenyl,cyclopentadienyl, and the like).

“Cycloalkyl” refers to a cyclic, bicyclic, tricyclic, or polycyclicnon-aromatic hydrocarbon groups having 3 to 12 carbons. Anysubstitutable ring atom can be substituted (e.g., by one or moresubstituents). The cycloalkyl groups can contain fused or Spiro rings.Fused rings are rings that share a common carbon atom. Examples ofcycloalkyl moieties include, but are not limited to, cyclopropyl,cyclohexyl, methylcyclohexyl, adamantyl, and norbornyl.

“Cycloalkylalkyl” refers to a -(cycloalkyl)-alkyl radical wherecycloalkyl and alkyl are as disclosed herein. The “cycloalkylalkyl” isbonded to the parent molecular structure through the cycloalkyl group.

“Heteroaromatic ring system” is art-recognized and refers to monocyclic,bicyclic or polycyclic ring system wherein at least one ring is botharomatic and comprises at least one heteroatom (e.g., N, O or S); andwherein no other rings are heterocyclyl (as defined below). In certaininstances, a ring which is aromatic and comprises a heteroatom contains1, 2, 3, or 4 ring heteroatoms in such ring.

“Heteroaryl” refers to a monovalent radical of a heteroaromatic ringsystem. Representative heteroaryl groups include ring systems where (i)each ring comprises a heteroatom and is aromatic, e.g., imidazolyl,oxazolyl, thiazolyl, triazolyl, pyrrolyl, furanyl, thiophenyl,pyrazolyl, pyridinyl, pyrazinyl, pyridazinyl, pyrimidinyl, indolizinyl,purinyl, naphthyridinyl, and pteridinyl; (ii) each ring is aromatic orcarbocyclyl, at least one aromatic ring comprises a heteroatom and atleast one other ring is a hydrocarbon ring or e.g., indolyl, isoindolyl,benzothienyl, benzofuranyl, dibenzofuranyl, indazolyl, benzimidazolyl,benzthiazolyl, quinolyl, isoquinolyl, cinnolinyl, phthalazinyl,quinazolinyl, quinoxalinyl, carbazolyl, acridinyl, phenazinyl,phenothiazinyl, phenoxazinyl, pyrido[2,3-b]-1,4-oxazin-3-(4H)-one,5,6,7,8-tetrahydroquinolinyl and 5,6,7,8-tetrahydroisoquinolinyl; and(iii) each ring is aromatic or carbocyclyl, and at least one aromaticring shares a bridgehead heteroatom with another aromatic ring, e.g.,4H-quinolizinyl.

“Heterocyclic ring system” refers to monocyclic, bicyclic and polycyclicring systems where at least one ring is saturated or partiallyunsaturated (but not aromatic) and that ring comprises at least oneheteroatom. A heterocyclic ring system can be attached to its pendantgroup at any heteroatom or carbon atom that results in a stablestructure and any of the ring atoms can be optionally substituted.

“Heterocyclyl” refers to a monovalent radical of a heterocyclic ringsystem. Representative heterocyclyls include ring systems in which (i)every ring is non-aromatic and at least one ring comprises a heteroatom,e.g., tetrahydrofuranyl, tetrahydropyranyl, tetrahydrothienyl,pyrrolidinyl, pyrrolidonyl, piperidinyl, pyrrolinyl,decahydroquinolinyl, oxazolidinyl, piperazinyl, dioxanyl, dioxolanyl,diazepinyl, oxazepinyl, thiazepinyl, morpholinyl, and quinuclidinyl;(ii) at least one ring is non-aromatic and comprises a heteroatom and atleast one other ring is an aromatic carbon ring, e.g.,1,2,3,4-tetrahydroquinolinyl, 1,2,3,4-tetrahydroisoquinolinyl; and (iii)at least one ring is non-aromatic and comprises a heteroatom and atleast one other ring is aromatic and comprises a heteroatom, e.g.,3,4-dihydro-1H-pyrano[4,3-c]pyridine, and1,2,3,4-tetrahydro-2,6-naphthyridine.

“Heterocyclylalkyl” refers to an alkyl group substituted with aheterocyclyl group.

“Cyano” refers to a —CN radical.

“Nitro” refers to —NO₂.

“Hydroxy” or “hydroxyl” refers to —OH.

As used herein, the definition of each expression, e.g., alkyl, m, n,etc., when it occurs more than once in any structure, is intended to beindependent of its definition elsewhere in the same structure.

Certain compounds of the present invention may exist in particulargeometric or stereoisomeric forms. The present invention contemplatesall such compounds, including cis- and trans-isomers, R- andS-enantiomers, diastereomers, (D)-isomers, (L)-isomers, the racemicmixtures thereof, and other mixtures thereof, as falling within thescope of the invention. Additional asymmetric carbon atoms may bepresent in a substituent such as an alkyl group. All such isomers, aswell as mixtures thereof, are intended to be included in this invention.

If, for instance, a particular enantiomer of compound of the presentinvention is desired, it may be prepared by asymmetric synthesis, or byderivation with a chiral auxiliary, where the resulting diastereomericmixture is separated and the auxiliary group cleaved to provide the puredesired enantiomers. Alternatively, where the molecule contains a basicfunctional group, such as amino, or an acidic functional group, such ascarboxyl, diastereomeric salts are formed with an appropriateoptically-active acid or base, followed by resolution of thediastereomers thus formed by fractional crystallization orchromatographic means well known in the art, and subsequent recovery ofthe pure enantiomers.

Unless otherwise indicated, when a disclosed compound is named ordepicted by a structure without specifying the stereochemistry and hasone or more chiral centers, it is understood to represent all possiblestereoisomers of the compound, as well as enantiomeric mixtures thereof.

The “enantiomeric excess” or “% enantiomeric excess” of a compositioncan be calculated using the equation shown below. In the example shownbelow a composition contains 90% of one enantiomer, e.g., the Senantiomer, and 10% of the other enantiomer, i.e., the R enantiomer.

ee=(90−10)/100=80%.

Thus, a composition containing 90% of one enantiomer and 10% of theother enantiomer is said to have an enantiomeric excess of 80%.

The compounds or compositions described herein may contain anenantiomeric excess of at least 50%, 75%, 90%, 95%, or 99% of one formof the compound, e.g., the S-enantiomer. In other words such compoundsor compositions contain an enantiomeric excess of the S enantiomer overthe R enantiomer.

The compounds described herein may also contain unnatural proportions ofatomic isotopes at one or more of the atoms that constitute suchcompounds. For example, the compounds may be radiolabeled withradioactive isotopes, such as for example deuterium (²H), tritium (³H),carbon-13 (¹³C), or carbon-14 (¹⁴C). All isotopic variations of thecompounds disclosed herein, whether radioactive or not, are intended tobe encompassed within the scope of the present invention. In addition,all tautomeric forms of the compounds described herein are intended tobe within the scope of the invention.

The compound can be useful as the free base or as a salt. Representativesalts include the hydrobromide, hydrochloride, sulfate, bisulfate,phosphate, nitrate, acetate, valerate, oleate, palmitate, stearate,laurate, benzoate, lactate, phosphate, tosylate, citrate, maleate,fumarate, succinate, tartrate, naphthylate, mesylate, glucoheptonate,lactobionate, and laurylsulphonate salts and the like. (See, forexample, Berge et al. (1977) “Pharmaceutical Salts”, J. Pharm. Sci.66:1-19.)

As described herein, compounds of the invention may contain “optionallysubstituted” moieties. In general, the term “substituted”, whetherpreceded by the term “optionally” or not, means that one or morehydrogens of the designated moiety are replaced with a suitablesubstituent. Unless otherwise indicated, an “optionally substituted”group may have a suitable substituent at each substitutable position ofthe group, and when more than one position in any given structure may besubstituted with more than one substituent selected from a specifiedgroup, the substituent may be either the same or different at eachposition. Combinations of substituents envisioned under this inventionare preferably those that result in the formation of stable orchemically feasible compounds. The term “stable”, as used herein, refersto compounds that are not substantially altered when subjected toconditions to allow for their production, detection, and, in certainembodiments, their recovery, purification, and use for one or more ofthe purposes disclosed herein.

Suitable substituents for an optionally substituted alkyl, alkylene,heteroalkyl, heteroalkylene, carbocyclyl, heterocyclyl, aryl group andheteroaryl group include halogen, ═O, —CN, —OR^(c), —NR^(d)R^(e),—S(O)_(k)R^(c), —NR^(c)S(O)₂R^(c), —S(O)₂NR^(d)R^(e), —C(═O)OR^(c),—OC(═O)OR^(c), —OC(═O)R^(c), —OC(═S)OR^(c), —C(═S)OR^(c), —O(C═S)R^(c),—C(═O)NR^(d)R^(e), —NR^(c)C(═O)R^(c), —C(═S)NR^(d)R^(e),—NR^(c)C(═S)R^(c), —NR^(c)(C═O)OR^(c), —O(C═O)NR^(d)R^(e),—NR^(c)(C═S)OR^(c), —O(C═S)NR^(d)R^(e), —NR^(c)(C═O)NR^(d)R^(e),—NR^(c)(C═S)NR^(d)R^(e), —C(═S)R^(c), —C(═O)R^(c), C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ heteroalkyl, carbocyclyl, (C₁-C₆-alkylene)-carbocyclyl,(C₁-C₆-heteroalkylene)-carbocyclyl, heterocyclyl,(C₁-C₆-alkylene)-heterocyclyl, (C₁-C₆-heteroalkylene)-heterocyclyl,aryl, (C₁-C₆-alkylene)-aryl, (C₁-C₆-heteroalkylene)-aryl, heteroaryl,(C₁-C₆-alkylene)-heteroaryl, or (C₁-C₆-heteroalkylene)-heteroaryl,wherein each of said alkyl, alkylene, heteroalkyl, heteroalkylene,carbocyclyl, heterocyclyl, aryl and heteroaryl are optionallysubstituted with one or more of halogen, OR^(c), —NO₂, —CN,—NR^(c)C(═O)W, —NR^(d)R^(e), —S(O)_(k)R^(c), —C(═O)OR^(c),—C(═O)NR^(d)R^(e), —C(═O)R^(c), C₁-C₆ alkyl, C₁-C₆ haloalkyl, or C₁-C₆heteroalkyl, and wherein R^(c) is hydrogen, hydroxy, C₁-C₆ alkyl, C₁-C₆heteroalkyl, carbocyclyl, (C₁-C₆-alkylene)-carbocyclyl,(C₁-C₆-heteroalkylene)-carbocyclyl, heterocyclyl,(C₁-C₆-alkylene)-heterocyclyl, (C₁-C₆-heteroalkylene)-heterocyclyl,aryl, (C₁-C₆-alkylene)-aryl, (C₁-C₆-heteroalkylene)-aryl, heteroaryl,(C₁-C₆-alkylene)-heteroaryl, or (C₁-C₆-heteroalkylene)-heteroaryl, eachof which is optionally substituted with one or more of halogen, hydroxy,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ heteroalkyl, carbocyclyl,heterocyclyl, aryl, or heteroaryl; R^(d) and R^(e) are eachindependently selected from hydrogen, C₁-C₆ alkyl, or C₁-C₆ heteroalkyl;and k is 0, 1 or 2. The invention is not intended to be limited in anymanner by the above exemplary listing of substituents.

TABLE 1 Exemplary Compounds of the Invention. Compound Structure 100

101

102

103

104

105

106

107

108

109

110

111

112

113

114

115

116

117

118

119

120

121

122

123

124

125

126

127

128

129

130

131

132

133

134

135

136

137

138

139

140

141

142

143

144

145

146

147

148

149

150

151

Pharmaceutically acceptable salts of these compounds are alsocontemplated for the uses described herein.

“Pharmaceutically acceptable salt” refers to any salt of a compound ofthe invention which retains its biological properties and which is nottoxic or otherwise undesirable for pharmaceutical use. Pharmaceuticallyacceptable salts may be derived from a variety of organic and inorganiccounter-ions well known in the art and include. Such salts include: (1)acid addition salts formed with organic or inorganic acids such ashydrochloric, hydrobromic, sulfuric, nitric, phosphoric, sulfamic,acetic, trifluoroacetic, trichloroacetic, propionic, hexanoic,cyclopentylpropionic, glycolic, glutaric, pyruvic, lactic, malonic,succinic, sorbic, ascorbic, malic, maleic, fumaric, tartaric, citric,benzoic, 3-(4-hydroxybenzoyl)benzoic, picric, cinnamic, mandelic,phthalic, lauric, methanesulfonic, ethanesulfonic,1,2-ethane-disulfonic, 2-hydroxyethanesulfonic, benzenesulfonic,4-chlorobenzenesulfonic, 2-naphthalenesulfonic, 4-toluenesulfonic,camphoric, camphorsulfonic,4-methylbicyclo[2.2.2]-oct-2-ene-1-carboxylic, glucoheptonic,3-phenylpropionic, trimethylacetic, tert-butylacetic, lauryl sulfuric,gluconic, benzoic, glutamic, hydroxynaphthoic, salicylic, stearic,cyclohexylsulfamic, quinic, muconic acid and the like acids; or (2)salts formed when an acidic proton present in the parent compound either(a) is replaced by a metal ion, e.g., an alkali metal ion, an alkalineearth ion or an aluminum ion, or alkali metal or alkaline earth metalhydroxides, such as sodium, potassium, calcium, magnesium, aluminum,lithium, zinc, and barium hydroxide, ammonia or (b) coordinates with anorganic base, such as aliphatic, alicyclic, or aromatic organic amines,such as ammonia, methylamine, dimethylamine, diethyl amine, picoline,ethanol amine, diethanolamine, triethanolamine, ethylenediamine, lysine,arginine, ornithine, choline, N,N′-dibenzylethylene-diamine,chloroprocaine, diethanolamine, procaine, N-benzylphenethylamine,N-methylglucamine piperazine, tris(hydroxymethyl)-aminomethane,tetramethylammonium hydroxide, and the like. Pharmaceutically acceptablesalts further include, by way of example only, sodium, potassium,calcium, magnesium, ammonium, tetraalkylammonium and the like, and whenthe compound contains a basic functionality, salts of non-toxic organicor inorganic acids, such as hydrochloride, hydrobromide, tartrate,mesylate, besylate, acetate, maleate, oxalate and the like.

Pharmaceutical Compositions

Pharmaceutical compositions of the invention comprise one or morecompounds of the invention and one or more physiologically orpharmaceutically acceptable carrier. The term “pharmaceuticallyacceptable carrier” refers to a pharmaceutically-acceptable material,composition or vehicle, such as a liquid or solid filler, diluent,excipient, solvent or encapsulating material, involved in carrying ortransporting any subject composition or component thereof. Each carriermust be “acceptable” in the sense of being compatible with the subjectcomposition and its components and not injurious to the patient. Someexamples of materials which may serve as pharmaceutically acceptablecarriers include: (1) sugars, such as lactose, glucose and sucrose; (2)starches, such as corn starch and potato starch; (3) cellulose, and itsderivatives, such as sodium carboxymethyl cellulose, ethyl cellulose andcellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7)talc; (8) excipients, such as cocoa butter and suppository waxes; (9)oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil,olive oil, corn oil and soybean oil; (10) glycols, such as propyleneglycol; (11) polyols, such as glycerin, sorbitol, mannitol andpolyethylene glycol; (12) esters, such as ethyl oleate and ethyllaurate; (13) agar; (14) buffering agents, such as magnesium hydroxideand aluminum hydroxide; (15) alginic acid; (16) pyrogen-free water; (17)isotonic saline; (18) Ringer's solution; (19) ethyl alcohol; (20)phosphate buffer solutions; and (21) other non-toxic compatiblesubstances employed in pharmaceutical formulations.

The compositions of the invention may be administered orally,parenterally, by inhalation spray, topically, rectally, nasally,buccally, vaginally or via an implanted reservoir. The term “parenteral”as used herein includes subcutaneous, intravenous, intramuscular,intra-articular, intra-synovial, intrasternal, intrathecal,intrahepatic, intralesional and intracranial injection or infusiontechniques. In some embodiments, the compositions of the invention areadministered orally, intraperitoneally or intravenously. Sterileinjectable forms of the compositions of this invention may be aqueous oroleaginous suspension. These suspensions may be formulated according totechniques known in the art using suitable dispersing or wetting agentsand suspending agents. The sterile injectable preparation may also be asterile injectable solution or suspension in a non-toxic parenterallyacceptable diluent or solvent, for example as a solution in1,3-butanediol. Among the acceptable vehicles and solvents that may beemployed are water, Ringer's solution and isotonic sodium chloridesolution. In addition, sterile, fixed oils are conventionally employedas a solvent or suspending medium.

For this purpose, any bland fixed oil may be employed includingsynthetic mono- or di-glycerides. Fatty acids, such as oleic acid andits glyceride derivatives are useful in the preparation of injectables,as are natural pharmaceutically-acceptable oils, such as olive oil orcastor oil, especially in their polyoxyethylated versions. These oilsolutions or suspensions may also contain a long-chain alcohol diluentor dispersant, such as carboxymethyl cellulose or similar dispersingagents that are commonly used in the formulation of pharmaceuticallyacceptable dosage forms including emulsions and suspensions. Othercommonly used surfactants, such as Tween, Spans and other emulsifyingagents or bioavailability enhancers which are commonly used in themanufacture of pharmaceutically acceptable solid, liquid, or otherdosage forms may also be used for the purposes of formulation.

The pharmaceutically acceptable compositions of this invention may beorally administered in any orally acceptable dosage form including, butnot limited to, capsules, tablets, aqueous suspensions or solutions. Inthe case of tablets for oral use, carriers commonly used include lactoseand corn starch. Lubricating agents, such as magnesium stearate, arealso typically added. For oral administration in a capsule form, usefuldiluents include lactose and dried cornstarch. When aqueous suspensionsare required for oral use, the active ingredient is combined withemulsifying and suspending agents. If desired, certain sweetening,flavoring or coloring agents may also be added.

Alternatively, the pharmaceutically acceptable compositions of thisinvention may be administered in the form of suppositories for rectaladministration. These can be prepared by mixing the agent with asuitable non-irritating excipient that is solid at room temperature butliquid at rectal temperature and therefore will melt in the rectum torelease the drug. Such materials include cocoa butter, beeswax andpolyethylene glycols.

The pharmaceutically acceptable compositions of this invention may alsobe administered topically, especially when the target of treatmentincludes areas or organs readily accessible by topical application,including diseases of the eye, the skin, or the lower intestinal tract.Suitable topical formulations are readily prepared for each of theseareas or organs. Topical application for the lower intestinal tract canbe effected in a rectal suppository formulation (see above) or in asuitable enema formulation. Topically-transdermal patches may also beused.

For topical applications, the pharmaceutically acceptable compositionsmay be formulated in a suitable ointment containing the active componentsuspended or dissolved in one or more carriers. Carriers for topicaladministration of the compounds of this invention include, but are notlimited to, mineral oil, liquid petrolatum, white petrolatum, propyleneglycol, polyoxyethylene, polyoxypropylene compound, emulsifying wax andwater. Alternatively, the pharmaceutically acceptable compositions canbe formulated in a suitable lotion or cream containing the activecomponents suspended or dissolved in one or more pharmaceuticallyacceptable carriers. Suitable carriers include, but are not limited to,mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax,cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.

The pharmaceutically acceptable compositions of this invention may alsobe administered by nasal aerosol or inhalation. Such compositions areprepared according to techniques well-known in the art of pharmaceuticalformulation and may be prepared as solutions in saline, employing benzylalcohol or other suitable preservatives, absorption promoters to enhancebioavailability, fluorocarbons, and/or other conventional solubilizingor dispersing agents.

The amount of the compounds of the present invention that may becombined with the carrier materials to produce a composition in a singledosage form will vary depending upon the host treated, the particularmode of administration.

Dosages

Toxicity and therapeutic efficacy of compounds of the invention,including pharmaceutically acceptable salts and deuterated variants, canbe determined by standard pharmaceutical procedures in cell cultures orexperimental animals. The LD₅₀ is the dose lethal to 50% of thepopulation. The ED₅₀ is the dose therapeutically effective in 50% of thepopulation. The dose ratio between toxic and therapeutic effects(LD₅₀/ED₅₀) is the therapeutic index. Compounds that exhibit largetherapeutic indexes are preferred. While compounds that exhibit toxicside effects may be used, care should be taken to design a deliverysystem that targets such compounds to the site of affected tissue inorder to minimize potential damage to uninfected cells and, thereby,reduce side effects.

Data obtained from the cell culture assays and animal studies can beused in formulating a range of dosage for use in humans. The dosage ofsuch compounds may lie within a range of circulating concentrations thatinclude the ED₅₀ with little or no toxicity. The dosage may vary withinthis range depending upon the dosage form employed and the route ofadministration utilized. For any compound, the therapeutically effectivedose can be estimated initially from cell culture assays. A dose may beformulated in animal models to achieve a circulating plasmaconcentration range that includes the IC₅₀ (i.e., the concentration ofthe test compound that achieves a half-maximal inhibition of symptoms)as determined in cell culture. Such information can be used to moreaccurately determine useful doses in humans. Levels in plasma may bemeasured, for example, by high performance liquid chromatography.

It should also be understood that a specific dosage and treatmentregimen for any particular patient will depend upon a variety offactors, including the activity of the specific compound employed, theage, body weight, general health, sex, diet, time of administration,rate of excretion, drug combination, and the judgment of the treatingphysician and the severity of the particular disease being treated. Theamount of a compound of the present invention in the composition willalso depend upon the particular compound in the composition.

Treatment

RET fusions have been implicated in several types of cancers. Generally,these RET fusions have a RET kinase domain that is the same as inwild-type RET; therefore, as used herein, any RET protein with the samekinase domain as wild-type RET will be referred to as “wild-type RET.”Mutations can occur in the RET kinase domain, leading to resistantmutants of RET.

The activity of exemplary compounds that are approved or in developmentfor RET-related conditions is shown below. As shown, the compounds areactive against the wild-type RET, but are much less active against themutated forms.

RET wt RET V804L Biochemical Biochemical Compound IC₅₀ (nM) IC₅₀ (nM)Cabozantinib 11 45 Vandetanib 4 3597 Sorafenib 7.9 95.2 Regorafenib 1253

The invention provides compounds that inhibit both wild-type RET andmutants of RET, e.g., mutants of RET that are resistant to currentstandard of care treatments (“RET resistant mutants”). In addition, thecompounds of the invention can be selective for wild-type RET, overother kinases, thus leading to reduced toxicities associated withinhibiting other kinases.

Mutations can be predicted using structural biology and computationalanalyses, as well as by examining codon sequences in which a sequencechange gives rise to a codon for a different amino acid. Using suchmethods, RET resistant mutants are predicted to have point mutations atthe 804 gatekeeper residue in the RET protein and/or at residues at ornear the gatekeeper residue. In some embodiments, the mutation may be atone or more of the 804, 806, 810, 865, 870, 891, and 918 residues.Specific examples of RET resistant mutants include: V804L, V804M, V804E,Y806C, Y806S, Y806H, Y806N, G810R, G810S, L865V, L870F, S891A and M918Tmutants.

Mutations occurring from administration of a particular inhibitor (e.g.,a known RET wild-type inhibitor) can be determined experimentally byexposing cells to a mutation-promoting agent, such as ENU. The cells arewashed, then plated with increasing concentrations (2-100× proliferationIC₅₀) of the compound of choice. The wells with cellular outgrowth arethen collected after 3-4 weeks. The RET kinase domain is then sequencedto identify resistance mutations (i.e., altered forms of the RET proteinthat retain enzymatic activity). Resistance can be confirmed by exposingthese cells with the compound of choice. Resistant mutants that havebeen identified experimentally include the V804L, V804E, V804M, andY806H mutants.

Because of their activity against wild-type RET and mutant RET, thecompounds described herein can be used to treat a patient with acondition associated with aberrant RET activity. They can also be usedto treat various cancers. In some embodiments, the cancer is selectedfrom papillary thyroid carcinoma (PTC), medullary thyroid cancer (MTC),pheochromocytoma (PC), pancreatic ductal adenocarcinoma, multipleendocrine neoplasia (MEN2A and MEN2B), metastatic breast cancer,testicular cancer, small cell lung cancer, non-small cell lung cancer,chronic myelomonocytic leukemia, colorectal cancer, ovarian cancer, andcancers of the salivary gland.

The compounds can also be used to treat a patient who has developedresistance to a wild-type RET inhibitor, or a patient with a particularRET mutant. The method includes the step of administering a compound orcomposition of the invention that is active against one or more RETresistant mutants. In certain embodiments, the RET resistant mutant isselected from V804L, V804M, V804E, Y806C, Y806S, Y806N, Y806H, G810R,G810S, L865V, L870F, S891A and M918T. By “active” is meant that acompound has an IC₅₀ of less than 1 μM, 500 nM, 250 nM, 100 nM, 75 nM,50 nM, 25 nM, 10 nM, or 5 nM when measured in a biochemical assay,against at least one resistant mutant.

The compounds and compositions described herein can be administeredalone or in combination with other compounds, including otherRET-modulating compounds, or other therapeutic agents. In someembodiments, the compound or composition of the invention may beadministered in combination with one or more compounds selected fromCabozantinib (COMETRIQ), Vandetanib (CALPRESA), Sorafenib (NEXAVAR),Sunitinib (SUTENT), Regorafenib (STAVARGA), Ponatinib (ICLUSIG),Bevacizumab (AVASTIN), Crizotinib (XALKORI), or Gefitinib (IRESSA). Thecompound or composition of the invention may be administeredsimultaneously or sequentially with the other therapeutic agent by thesame of different routes of administration. The compound of theinvention may be included in a single formulation with the othertherapeutic agent or in separate formulations.

EXAMPLES

The following examples are intended to be illustrative, and are notmeant in any way to be limiting.

Compounds of the invention, including salts and N-oxides thereof, can beprepared using known organic synthesis techniques and can be synthesizedaccording to any of numerous possible synthetic routes, such as those inthe Synthetic Protocols below and in the Examples. The below Schemes aremeant to provide general guidance in connection with preparing thecompounds of the invention. One skilled in the art would understand thatthe preparations shown in the Schemes can be modified or optimized usinggeneral knowledge of organic chemistry to prepare various compounds ofthe invention.

Synthetic Protocol 1:

An aryl dihalide may be treated with an organolithium or organomagnesiumhalide reagent, such as n-BuLi or i-PrMgCl, and the arylmetal reagentmay then undergo addition to an ester substituted cyclohexanone (eithercommercially available or prepared as described in “Synthesis of Ketoneand Boronate Intermediates”). The remaining halide can then undergo acoupling reaction with an arylamine under SnAr conditions ormetal-catalyzed coupling conditions to give a tricyclic esterintermediate. The ester can then be hydrolyzed under basic conditions togive an acid, which can then undergo an amide coupling reaction with anamine (either commercially available or prepared as described in“Synthesis of Amine Intermediates”). The amides are examples of RETinhibitors described herein, but can also be further modified. Forexample, the tertiary alcohol can be treated with a fluorinating reagentsuch as DAST to give a mixture of deoxyfluorinated products anddehydrated products. The dehydrated products can be reduced undertypical hydrogenation conditions such as Pd and H₂, or Pd and ammoniumformate to give the reduced products which are also examples of RETinhibitors.

Synthetic Protocol 2:

The heteroaryl dihalide can be coupled to an amino pyrazole undernucleophilic aromatic substitution reaction conditions using a base suchas diisopropylethylamine (DIPEA) or triethylamine (TEA) in a polarsolvent to provide the bicyclic ring system. The bicyclic heteroarylhalide can then be coupled to a to a boron, tin or zinc alkenyl or alkylreagent via a

Palladium-mediated coupling reaction, e.g., Suzuki, Stille, Negishicoupling, to provide the tricyclic ring system. For example, inSynthetic Protocol 2, the bicyclic heteroaryl halide of the can becoupled to a variety of ester substituted cyclohexenyl boronic esters(commercially available or those described under the heading “Synthesisof Vinyl Boronates”) under Suzuki coupling reaction conditions (X=halo,e.g., chloro; and M=B(OR)₂) to provide the tricyclic carboxylic esterintermediate. The carboxylic ester can then be hydrolyzed under acidicor basic conditions to provide a carboxylic acid intermediate. Thecarboxylic acid intermediate can then be coupled to a variety of amineintermediates, such as those described in Example 9 to provide the amidefinal product.

Synthetic Protocol 3:

A substituted cycloalkyl iodide (either commercially available orprepared as described in “Synthesis of Iodide Intermediates”) wastreated with activated zinc. The zinc was then activated by a varietymethods, including but not limited to the method of Reike or treatmentwith TMS-Cl and 1,2-dibromoethane. The cycloalkyl zinc reagent can thenbe coupled to a heteroaryl halide with palladium catalysis under Negishicoupling conditions. The thiomethyl group of the resulting product canthen be converted to a chloride via oxidation to the sulfone, hydrolysisunder acidic conditions, and chlorination with POCl₃ or oxalyl chloride.The heteroaryl chloride can then undergo displacement with an aryl amineunder either SnAr conditions or palladium mediated coupling conditions.The tricyclic carboxylic ester can then be hydrolyzed under acidic orbasic conditions to provide a carboxylic acid intermediate. Thecarboxylic acid intermediate can then be coupled to a variety of aminesintermediates, such as those described in Example 9 to provide the amidefinal product.

Synthetic Protocol 4:

A substituted cycloalkyl iodide (either commercially available orprepared as described in “Synthesis of Iodide Intermediates”) wastreated with activated zinc. The zinc could be activated by a varietymethods, including but not limited to the method of Reike or treatmentwith TMS-Cl and 1,2-dibromoethane. The cycloalkyl zinc reagent can thenbe coupled to a heteroaryl dihalide with palladium catalysis underNegishi coupling conditions. The remaining halide group of the resultingproduct can then undergo displacement with an aryl amine under eitherSnAr conditions or palladium mediated coupling conditions. The arylamine can either be unprotected or the pyrazole N—H can be protectedwith a variety of groups, such as Boc. The tricyclic carboxylic estercan then be hydrolyzed under acidic or basic conditions to provide acarboxylic acid intermediate, which also removes the protecting groupfrom the pyrazole. The carboxylic acid intermediate can then be coupledto a variety of amines intermediates, such as those described in“Synthesis of Amine Intermediates” to provide the amide final product.

The reactions for preparing compounds of the invention can be carriedout in suitable solvents which can be readily selected by one of skillin the art of organic synthesis. Suitable solvents can be substantiallynon-reactive with the starting materials (reactants), the intermediates,or products at the temperatures at which the reactions are carried out,e.g., temperatures which can range from the solvent's freezingtemperature to the solvent's boiling temperature. A given reaction canbe carried out in one solvent or a mixture of more than one solvent.Depending on the particular reaction step, suitable solvents for aparticular reaction step can be selected by the skilled artisan.

Preparation of compounds of the invention can involve the protection anddeprotection of various chemical groups. The need for protection anddeprotection, and the selection of appropriate protecting groups, can bereadily determined by one skilled in the art. The chemistry ofprotecting groups can be found, for example, in Wuts and Greene,Protective Groups in Organic Synthesis, 5th ed., John Wiley & Sons: NewJersey, (2014), which is incorporated herein by reference in itsentirety.

Reactions can be monitored according to any suitable method known in theart. For example, product formation can be monitored by spectroscopicmeans, such as nuclear magnetic resonance (NMR) spectroscopy (e.g., ¹Hor ¹³C), infrared (IR) spectroscopy, spectrophotometry (e.g.,UV-visible), mass spectrometry (MS), or by chromatographic methods suchas high performance liquid chromatography (HPLC) or thin layerchromatography (TLC). Analytical instruments and methods for compoundcharacterization:

LC-MS:

Unless otherwise indicated, all liquid chromatography-mass spectrometry(LC-MS) data (sample analyzed for purity and identity) were obtainedwith an Agilent model-1260 LC system using an Agilent model 6120 massspectrometer utilizing ES-API ionization fitted with an Agilent Poroshel120 (EC-C18, 2.7 um particle size, 3.0×50 mm dimensions) reverse-phasecolumn at 22.4 degrees Celsius. The mobile phase consisted of a mixtureof solvent 0.1% formic acid in water and 0.1% formic acid inacetonitrile. A constant gradient from 95% aqueous/5% organic to 5%aqueous/95% organic mobile phase over the course of 4 minutes wasutilized. The flow rate was constant at 1 mL/min.

Prep LC-MS:

Preparative HPLC was performed on a Shimadzu Discovery VP® Preparativesystem fitted with a Luna 5u C18(2) 100A, AXIA packed, 250×21.2 mmreverse-phase column at 22.4 degrees Celsius. The mobile phase consistedof a mixture of solvent 0.1% formic acid in water and 0.1% formic acidin acetonitrile. A constant gradient from 95% aqueous/5% organic to 5%aqueous/95% organic mobile phase over the course of 25 minutes wasutilized. The flow rate was constant at 20 mL/min. Reactions carried outin a microwave were done so in a Biotage Initiator microwave unit.

Silica Gel Chromatography:

Silica gel chromatography was performed on either a Teledyne IscoCombiFlash® Rf unit or a Biotage® Isolera Four unit.

Proton NMR:

Unless otherwise indicated, all NMR spectra were obtained with a Varian400 MHz Unity Inova 400 MHz NMR instrument (acquisition time=3.5 secondswith a 1 second delay; 16 to 64 scans). Where characterized, all protonswere reported in DMSO-d6 solvent as parts-per million (ppm) with respectto residual DMSO (2.50 ppm).

Example 1. Synthesis of Compounds 109 and 110 Step 1: Synthesis of(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 109) and(1S,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 110)

N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyridin-2-yl)cyclohex-3-enecarboxamide(50 mg, 0.10 mmol) and 10% Pd/C (20 mg) in MeOH (5 mL) was stirred atambient temperature under a H₂ atmosphere (1 atm) for 1 h. The mixturewas then filtered through a pad of celite, and the filtered solution wasconcentrated and purified by preparative HPLC to give both of titlecompounds(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 109; 10.0 mg, 19.9%) and(1S,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 110; 24.8 mg, 49.5%) as a white solid. MS (ES+) C₂₇H₃₁FN₈Orequires: 502, found: 503 [M+H]⁺.

(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 109)

¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.66 (s, 1H), 8.82 (s, 1H), 8.68 (d,1H, J=4.4 Hz), 8.39 (s, 1H), 8.35 (d, 1H, J=6.8 Hz), 7.92-7.86 (m, 3H),6.89 (s, 1H), 6.37 (s, 1H), 6.12 (s, 1H), 5.00-4.97 (m, 1H), 2.50-2.44(m, 1H), 2.40-2.15 (m, 7H), 1.90-1.85 (m, 4H), 1.55-1.45 (m, 4H), 1.40(d, 3H, J=6.4 Hz).

(1S,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 110)

¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.62 (s, 1H), 8.78 (s, 1H), 8.66 (d,1H, J=4.4 Hz), 8.38 (d, 1H, J=1.6 Hz), 8.23 (d, 1H, J=7.6 Hz), 7.93-7.84(m, 3H), 6.83 (s, 1H), 6.35 (s, 1H), 6.15 (s, 1H), 5.03-5.00 (m, 1H),2.59-2.50 (m, 1H), 2.50-2.46 (m, 1H), 2.14-2.02 (m, 6H), 2.02-1.84 (m,4H), 1.63-1.55 (m, 4H), 1.40 (d, 3H, J=7.6 Hz).

Example 2. Synthesis of Compound 112 Step 1: Synthesis of2-chloro-6-methyl-N-(5-methyl-1H-pyrazol-3-yl)pyrimidin-4-amine

A suspension of 2,4-dichloro-6-methyl-pyrimidine (120.00 g, 736.2 mmol,1.00 eq), 5-methyl-1H-pyrazol-3-amine (78.65 g, 0.81 mol, 1.10 eq) andDIPEA (142.72 g, 1.10 mol, 1.50 eq) in DMSO (400.00 mL) was heated at60° C. for 16 hrs, at which point TLC (PE/EA, 5:1, 1:1) analysis showedthe reaction was complete. The reaction mixture was cooled to 30° C.,poured into ice-water (800 mL), and the resulting mixture was extractedwith MTBE (800 mL×10). The combined organic layers were washed withwater (400 mL×3), brine (400 mL×3) and dried over Na₂SO₄. Afterfiltration, the filtrate was concentrated under reduced pressure and theresidue was recrystallized from DCM (10 mL/g) to afford2-chloro-6-methyl-N-(5-methyl-1H-pyrazol-3-yl)pyrimidin-4-amine (105.60g, 472.14 mmol, 64%) as a yellow solid. The structure was confirmed byLC-MS and NMR.

Step 2: Synthesis of ethyl4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohex-3-ene-1-carboxylate

A mixture of2-chloro-6-methyl-N-(5-methyl-1H-pyrazol-3-yl)pyrimidin-4-amine (0.530g, 2.37 mmol), ethyl4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarboxylate(0.664 g, 2.37 mmol), and potassium carbonate (0.819 g, 5.92 mmol) indioxane (8.89 ml) and water (2.96 ml) was sparged with nitrogen gas for10 min, then Pd(PPh₃)₄ (0.137 g, 0.118 mmol) was added and the reactionvessel was sealed. The reaction mixture was heated in a microwavereactor at 125° C. for 80 min, then cooled to ambient temperature andpartitioned between 5:1 DCM/IPA and water. The aqueous layer was furtherextracted with 5:1 DCM/IPA. The organic layers were combined and driedover sodium sulfate. The dried solution was filtered, concentrated, andpurified by silica gel chromatography (gradient elution, 0 to 10%methanol-DCM) to give ethyl4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohex-3-ene-1-carboxylate(646 mg, 80%) as a yellow solid. MS (ES+) C₁₈H₂₃N₅O₂ requires: 341,found: 342 [M+H]⁺.

Step 3: Synthesis of ethyl4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexane-1-carboxylate

Palladium on carbon (10 wt %, 0.125 g, 0.117 mmol) and ammonium formate(0.296 g, 4.69 mmol) were added to a solution of ethyl4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohex-3-enecarboxylate(0.40 g, 1.2 mmol) in ethanol (11.7 ml) and the resulting mixture washeated to 70° C. for 30 min. The reaction mixture was cooled to ambienttemperature, and filtered through celite, rinsing the celite withmethanol. The filtered solution was then concentrated onto silica geland purified by silica gel chromatography (gradient elution, 0 to 10%methanol-DCM) to give ethyl4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexane-1-carboxylateas a 3:1 mixture of cis:trans. MS (ES+) C₁₈H₂₅N₅O₂ requires: 343, found:344 [M+H]⁺.

Step 4: Synthesis of4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexane-1-carboxylicAcid

Lithium hydroxide monohydrate (0.029 g, 0.70 mmol) was added to asolution of ethyl4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxylate(0.12 g, 0.35 mmol) in THF (2.8 mL), EtOH (2.8 mL), and water at ambienttemperature. The reaction mixture was stirred for 6 h, then concentratedaqueous HCl (37%, 0.072 ml, 0.87 mmol) was added. The reaction mixturewas concentrated and carried forward in the next step.

Step 5: Synthesis of(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexane-1-carboxamide(Compound 112)

HATU (162 mg, 0.427 mmol) was added to a solution of crude4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxylicacid (72 mg, 0.23 mmol),(S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethanamine hydrochloridesalt (97 mg, 0.40 mmol), and DIM (0.34 mL, 1.9 mmol) in DMF (3.8 mL) atambient temperature. The reaction mixture was stirred for 10 min, thenwas partitioned between EtOAc and H₂O. The organic layer was washed withsaturated aqueous NaCl solution, dried over sodium sulfate, filtered,and concentrated. The residue was purified by silica gel chromatography(gradient elution 0 to 10% methanol-dichloromethane with 2%triethylamine added) to give(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexane-1-carboxamide(Compound 112; 26 mg, 13% yield) as a white solid. MS (ES+) C₂₆H₃₀FN₉Orequires: 503, found: 504 [M+H]⁺. ¹H NMR (500 MHz, DMSO-d6) δ 11.88 (s,1H), 9.48 (s, 1H), 8.66 (d, J=4.5 Hz, 1H), 8.38 (d, J=2.2 Hz, 1H), 8.30(d, J=7.7 Hz, 1H), 7.94-7.81 (m, 3H), 6.83 (s, 1H), 6.16 (s, 1H)5.02-4.93 (m, 1H), 2-57-2.49 (m, 1H), 2.26-2.16 (m, 7H), 1.99-1.92 (m,2H), 1.88-1.80 (m, 2H), 1.58-1.36 (m, 7H).

Example 3. Synthesis of Compound 120 Step 1: Synthesis of (1S,4S)-ethyl4-(6-bromo-4-methylpyridin-2-yl)-4-hydroxycyclohexanecarboxylate and(1R,4R)-ethyl4-(6-bromo-4-methylpyridin-2-yl)-4-hydroxycyclohexanecarboxylate

A solution of 2,6-dibromo-4-methylpyridine (1.00 g, 3.98 mmol) in DCM(30 mL) was cooled to −78° C., and n-BuLi (2.5 M, 1.74 mL, 4.37 mmol)was added dropwise to the above solution at −78° C. The solution wasstirred at −78° C. for 15 minutes, followed by addition of ethyl4-oxocyclohexanecarboxylate (811 mg, 4.77 mmol), and the resultantmixture was stirred at −78° C. for 30 min. The mixture was then quenchedby addition of saturated aqueous NH₄Cl solution and extracted with DCM.Organic layers were combined, dried over sodium sulfate, filtered, andconcentrated. The residue was purified by silica gel column (PE:EA=2:1)to give (1R,4R)-ethyl4-(6-bromo-4-methylpyridin-2-yl)-4-hydroxycyclohexanecarboxylate (lesspolar by TLC, 500 mg, 36.7%) as a white solid, MS (ES+) C₁₅H₂₀BrNO₃requires: 341, found: 342 [M+H]⁺, and (1S,4S)-ethyl4-(6-bromo-4-methylpyridin-2-yl)-4-hydroxycyclohexanecarboxylate (morepolar by TLC, 500 mg, 36.7%) as a white solid. MS (ES+) C₁₅H₂₀BrNO₃requires: 341, found: 342 [M+H]⁺.

Step 2: Synthesis of (1S,4S)-ethyl4-hydroxy-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxylate

A mixture of (1s, 4s)-ethyl4-(6-bromo-4-methylpyridin-2-yl)-4-hydroxycyclohexanecarboxylate (500mg, 1.46 mmol), 5-methyl-1H-pyrazol-3-amine (283 mg, 2.92 mmol),t-BuXPhos (185 mg, 0.438 mmol), Pd₂(dba)₃ (200 mg, 0.219 mmol) and KOAc(429 mg, 4.38 mmol) in DMF (2 mL) and toluene (10 mL) was heated to 140°C. for 2 h under microwave irradiation. After cooling to ambienttemperature, the mixture was concentrated and purified by silica gelcolumn (PE:EA=1:2) to give (1s,4s)-ethyl4-hydroxy-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxylate(80 mg, 15%) as a white solid. MS (ES+) C₁₉H₂₆N₄O₃ requires: 358, found:359 [M+H]⁺.

Step 3: Synthesis of(1S,4S)-4-hydroxy-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxylicAcid

To a solution of (1S,4S)-ethyl4-hydroxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyridin-2-yl)cyclohexanecarboxylate(80 mg, 0.2231 mmol) in MeOH (3 mL) was added 2 M aqueous NaOH (0.5 mL,1 mmol) at 25° C. The solution was stirred at 25° C. for 15 h and thenconcentrated to remove MeOH. The aqueous solution was acidified with 2 MHCl to bring the pH to 6, which resulted in formation of a precipitate.The precipitated solid was collected and dried to give(1S,4S)-4-hydroxy-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxylicacid (60 mg, 81%) as a yellow solid. MS (ES+) C₁₇H₂₂N₄O₃ requires: 330,found: 331 [M+H]⁺.

Step 4: Synthesis of(1s,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-hydroxy-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 120)

A mixture of(1S,4S)-4-hydroxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyridin-2-yl)cyclohexanecarboxylicacid (60 mg, 0.18 mmol),(S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethanamine hydrochloride(44.0 mg, 0.1816 mmol), HATU (69.0 mg, 0.1816 mmol) and DIEA (70.4 mg,0.545 mmol) in DMA (2 mL) was stirred at 25° C. for 2 h. The solutionwas concentrated and purified by preparative HPLC to give the titleproduct (40 mg, 43%) as a white solid. MS (ES+) C₂₇H₃₁FN₈O₂ requires:518, found: 519 [M+H]⁺. ¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.71 (br. s.,1H), 8.92 (br. s., 1H), 8.69 (d, 1H, J=4.4 Hz), 8.39 (d, 1H, J=2.0 Hz),8.31 (d, 1H, J=7.6 Hz), 7.95-7.87 (m, 3H), 6.83 (br. s., 1H), 6.79 (s,1H), 6.09 (br. s., 1H), 5.01-4.98 (m, 1H), 4.89 (s, 1H), 2.50-2.48 (m,1H), 2.21 (s, 3H), 2.20 (s, 3H), 2.00-1.75 (m, 4H), 1.65-1.50 (m, 4H),1.41 (d, 3H, J=7.2 Hz).

Example 4. Synthesis of Compounds 121 and 122 Step 1: Synthesis of(1s,4R)-4-fluoro-N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 121),(1R,4S)-4-fluoro-N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 122), andN—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohex-3-enecarboxamide

A mixture of(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-hydroxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyridin-2-yl)cyclohexanecarboxamide(120 mg, 0.23 mmol) in DCM (6 mL) was cooled to 0° C. DAST (111 mg, 0.69mmol) was added to the mixture at 0° C., and the resultant mixture wasstirred at 25° C. for 2 h. The mixture was concentrated and purified bypreparative HPLC to give the title compounds(1S,4R)-4-fluoro-N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 121; 6.1 mg, 5.08%) and(1R,4S)-4-fluoro-N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 122; 13.2 mg, 11.0%) as white solids. MS (ES+) C₂₇H₃₀F₂N₈Orequires: 520, found: 521 [M+H]⁺. Also gaveN—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohex-3-enecarboxamide(50 mg, 43.4%) as a white solid. MS (ES+) C₂₇H₂₉FN₈O requires: 500,found: 501 [M+H]⁺.

(1S,4R)-4-fluoro-N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 121)

¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.73 (s, 1H), 9.01 (d, 1H, J=2.8 Hz),8.69 (d, 1H, J=4.4 Hz), 8.41-8.38 (m, 2H), 7.95-7.87 (m, 3H), 6.92 (s,1H), 6.66 (s, 1H), 6.14 (s, 1H), 5.00 (q, 1H, J=7.2 Hz), 2.50-2.31 (m,1H), 2.21-2.21 (m, 6H), 2.21-1.74 (m, 8H), 1.41 (d, 3H, J=7.2 Hz).

(1R,4S)-4-fluoro-N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyridin-2-yl)cyclohexanecarboxamide(Compound 122)

¹H-NMR (400 MHz, DMSO-d6) δ ppm 11.65 (s, 1H), 9.01 (s, 1H), 8.65 (d,1H, J=4.4 Hz), 8.38-8.33 (m, 2H), 7.92-7.84 (m, 3H), 6.83 (s, 1H), 6.67(s, 1H), 6.30 (s, 1H), 5.04 (q, 1H, J=7.2 Hz), 2.70-2.50 (m, 3H), 2.20(s, 3H), 2.15 (s, 3H), 2.21-1.70 (m, 6H), 1.40 (d, 3H, J=7.2 Hz).

Example 5: Synthesis of Compounds 129 and 130 Step 1: Synthesis of2-chloro-4-methyl-6-(methylthio)pyrimidine

2,4-Dichloro-6-methylpyrimidine (20.0 g, 0.123 mol) was dissolved in THF(200 mL). MeSNa (20% aq, 43 g, 0.129 mol) was added dropwise at −5° C.,and the resulting mixture was stirred overnight at room temperature. H₂O(100 mL) and EtOAc (100 mL) were added, and the layers were separated.The organic layer was washed with brine (2×), dried over sodium sulfate,and concentrated to afford a yellow solid. The solid was washed by PE(100 mL) to afford target compound (9.1 g). MS (ES+) C₆H₇ClN₂S requires:174, found: 175 [M+H]⁺.

Step 2: Synthesis of Methyl1-methoxy-4-(4-methyl-6-(methylthio)pyrimidin-2-yl)cyclohexane-1-carboxylate

Methyl 4-iodo-1-methoxycyclohexanecarboxylate (1.35 g, 4.53 mmol) wasdissolved in dimethylacetamide (10 mL) in a pressure vessel under astream of N₂. Rieke Zinc (5.7 mL of a 50 mg/mL suspension in THF, 4.34mmol) was added quickly via syringe, and the vessel was capped andstirred at ambient temperature for 15 minutes. The vessel was openedunder a stream of N₂ and 2-chloro-4-methyl-6-(methylthio)pyrimidine (659mg, 3.8 mmol) was added followed by PdCl₂dppf (138 mg, 0.19 mmol). Thevessel was capped and heated to 80° C. for one hour, then cooled to roomtemperature. The reaction mixture was diluted with EtOAc, filteredthrough celite, and the filtrate was washed with H₂O (3×), brine, driedover sodium sulfate, filtered, and concentrated. The resulting residuewas purified by flash-column chromatography on silica gel (gradientelution, 0 to 30% EtOAc-hexanes) to give methyl1-methoxy-4-(4-methyl-6-(methylthio)pyrimidin-2-yl)cyclohexanecarboxylate(828 mg, 70%) as a colorless oil. The product was determined to be ˜3:2mixture of isomers by integration of the UV peaks in the LC/MS andintegration of NMR. MS (ES+) C₁₅H₂₂N₂O₃S requires: 310, found: 311[M+H]⁺.

Step 3: Synthesis of Methyl1-methoxy-4-(4-methyl-6-(methylsulfonyl)pyrimidin-2-yl)cyclohexane-1-carboxylate

Methyl1-methoxy-4-(4-methyl-6-(methylthio)pyrimidin-2-yl)cyclohexanecarboxylate(825 mg, 2.66 mmol) was dissolved in DCM (12 mL) followed by theaddition of mCPBA (1.10 g, 6.38 mmol) at ambient temperature. Thereaction mixture was stirred for 16 h, then an additional portion ofmCPBA was added (200 mg). After stirring for an additional 4 h, thereaction mixture was diluted with DCM and then washed with saturatedsodium bicarbonate solution. The washed solution was dried over sodiumsulfate, filtered, concentrated, and the resulting residue was purifiedby flash-column chromatography on silica gel (gradient elution, 0 to 60%ethyl acetate-hexane) to afford methyl1-methoxy-4-(4-methyl-6-(methylsulfonyl)pyrimidin-2-yl)cyclohexanecarboxylate(808 mg, 89%) as a colorless oil. MS (ES+) C₁₅H₂₂N₂O₅S requires: 342,found: 343 [M+H]⁺.

Step 4: Synthesis of Methyl4-(4-hydroxy-6-methylpyrimidin-2-yl)-1-methoxycyclohexane-1-carboxylate

Methyl1-methoxy-4-(4-methyl-6-(methylsulfonyl)pyrimidin-2-yl)cyclohexanecarboxylate(600 mg, 1.75 mmol) was dissolved in acetic acid (5 mL) and heated to80° C. for 1 h. The reaction mixture was then cooled to ambienttemperature, concentrated under reduced pressure, triturated with H₂O,and filtered. The solids were washed with additional H₂O and then driedunder reduced pressure to afford the title compound, methyl4-(4-hydroxy-6-methylpyrimidin-2-yl)-1-methoxycyclohexanecarboxylate(390 mg, 79%), as a pale yellow solid. MS (ES+) C₁₄H₂₀N₂O₄ requires:280, found: 281 [M+H]⁺.

Step 5: Synthesis of Methyl4-(4-chloro-6-methylpyrimidin-2-yl)-1-methoxycyclohexane-1-carboxylate

Methyl4-(4-hydroxy-6-methylpyrimidin-2-yl)-1-methoxycyclohexanecarboxylate(380 mg, 1.36 mmol) was suspended in POCl₃ (3.2 mL, 33.9 mmol) andheated to 100° C. for 2 h. The reaction mixture was then cooled toambient temperature, concentrated, and the residue was treated withcrushed ice. The resulting suspension was partitioned with DCM, and theorganic layer was extracted with saturated sodium bicarbonate solutionand dried over sodium sulfate. The dried solution was filtered,concentrated, and the resulting residue was purified by flash-columnchromatography on silica gel (gradient elution, 0 to 30% ethylacetate-hexanes) to give methyl4-(4-chloro-6-methylpyrimidin-2-yl)-1-methoxycyclohexanecarboxylate (344mg, 85%) as a pale orange oil that solidified on standing. MS (ES+)C₁₄H₁₉ClN₂O₃ requires: 298, found: 299 [M+H]⁺.

Step 6: Synthesis of Methyl1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexane-1-carboxylate

Methyl4-(4-chloro-6-methylpyrimidin-2-yl)-1-methoxycyclohexanecarboxylate (300mg, 1.00 mmol), 3-methyl-1-pyrazol-5-amine (146 mg, 1.51 mmol),di-tert-butyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2-yl)phosphine (85mg, 0.2 equiv.), Pd₂(dba)₃ (92 mg, 0.1 equiv.), and potassium acetate(394 mg, 4.02 mmol) were combined in a vial under nitrogen and 4 mLdioxane was added. The reaction mixture was heated to 100° C. for 1 h,then cooled to ambient temperature. The reaction mixture was dilutedwith EtOAc, filtered through celite, concentrated, and the resultingresidue was purified by flash-column chromatography on silica gel(gradient elution, 0 to 10% methanol-dichloromethane) to give methyl1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxylate(192 mg, 53%) as a tan-colored foam. MS (ES+) C₁₈H₂₅N₅O₃ requires: 359,found: 360 [M+H]⁺.

Step 7: Synthesis of(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxamide(Compound 129) and(1S,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxamide(Compound 130)

The title compounds were prepared from methyl1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxylate(192 mg, 0.53 mmol) using the same two-step procedure (hydrolysis andamide coupling) outlined in Synthetic Protocols 1 and 2, with PyBOP asthe amide coupling reagent instead of HATU. The products were initiallyisolated as a mixture of diastereomers (190 mg), which was thendissolved in 6 mL methanol and purified by SFC (ChiralPak AD-H 21×250mm, 40% MeOH containing 0.25% DEA in CO₂, 2.5 mL injections, 70 mL/min).Peak 1 was concentrated to give(1R,4S)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxamide(29 mg, 10%) as a white solid. Peak 2 was concentrated to give(1s,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-1-methoxy-4-(4-methyl-6-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-2-yl)cyclohexanecarboxamide(130 mg, 46%) as a white solid.

Example 6. Synthesis of Compound 149 Step 1: Synthesis of Methyl4-(2-chloro-6-methylpyrimidin-4-yl)-1-methoxycyclohexane-1-carboxylate

Methyl 4-iodo-1-methoxycyclohexanecarboxylate (3.37 g, 11.3 mmol) wasdissolved in dimethylacetamide (38 mL) in a pressure vessel under astream of N₂. Rieke Zinc (17.7 mL of a 50 mg/mL suspension in THF, 13.6mmol) was added quickly via syringe, and the vessel was capped andstirred at ambient temperature for 15 minutes. The vessel was openedunder a stream of N₂ and 2,4-dichloro-6-methylpyrimidine (1.84 g, 11.3mmol) was added followed by PdCl₂dppf (826 mg, 1.13 mmol). The vesselwas capped and heated to 80° C. for one hour, then cooled to roomtemperature. The reaction mixture was diluted with EtOAc, filteredthrough celite, and the filtrate was washed with H₂O (3×), brine, driedover sodium sulfate, filtered, and concentrated. The resulting residuewas purified by flash-column chromatography on silica gel (gradientelution, 0 to 50% EtOAc-hexanes) to give methyl4-(2-chloro-6-methylpyrimidin-4-yl)-1-methoxycyclohexane-1-carboxylate(74 mg, 2.2%) as a colorless oil. MS (ES+) C₁₄H₁₉ClN₂O₃ requires: 298,found: 299 [M+H]⁺.

Step 2: Synthesis of tert-Butyl3-((4-(4-methoxy-4-(methoxycarbonyl)cyclohexyl)-6-Methylpyrimidin-2-yl)amino)-5-methyl-1H-pyrazole-1-carboxylate

Methyl4-(2-chloro-6-methylpyrimidin-4-yl)-1-methoxycyclohexane-1-carboxylate(70.5 mg, 0.236 mmol), tert-butyl3-amino-5-methyl-1H-pyrazole-1-carboxylate (69.8 mg, 0.354 mmol),di-tert-butyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2-yl)phosphine (20.0mg, 0.2 equiv.), Pd₂(dba)₃ (21.6 mg, 0.1 equiv.), and potassium acetate(70 mg, 0.71 mmol) were combined in a vial under nitrogen and 0.98 mLdioxane was added. The reaction mixture was heated to 115° C. for 2 h,then cooled to ambient temperature. The reaction mixture was dilutedwith EtOAc, filtered through celite, concentrated onto silica gel, andthe resulting residue was purified by flash-column chromatography onsilica gel (gradient elution, 0 to 100% ethyl acetate-hexanes) to givetert-butyl3-((4-(4-methoxy-4-(methoxycarbonyl)cyclohexyl)-6-methylpyrimidin-2-yl)amino)-5-methyl-1H-pyrazole-1-carboxylate(48 mg, 44%) as a yellow oil. MS (ES+) C₂₃H₃₃N₅O₅ requires: 459, found:460 [M+H]⁺.

Step 3: Synthesis of1-Methoxy-4-(6-methyl-2-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-4-yl)cyclohexane-1-carboxylicAcid

Lithium hydroxide monohydrate (13 mg, 0.31 mmol) was added to a solutionof tert-butyl3-((4-(4-methoxy-4-(methoxycarbonyl)cyclohexyl)-6-methylpyrimidin-2-yl)amino)-5-methyl-1H-pyrazole-1-carboxylate(47.7 mg, 0.104 mmol) in THF/MeOH/H₂O (17:1:1, 1.8 mL). The reactionmixture was heated to 60° C. and stirred for 16 h. The reaction mixturewas then cooled to ambient temperature and concentrated to give crude1-methoxy-4-(6-methyl-2-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-4-yl)cyclohexane-1-carboxylicacid (57 mg, crude) which was used in the subsequent amide couplingwithout any further purification. MS (ES+) C₁₇H₂₃N₅O₃ requires: 345,found: 346 [M+H]⁺.

Step 4: Synthesis of(1s,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-1-methoxy-4-(6-methyl-2-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-4-yl)cyclohexane-1-carboxamide(Compound 149)

The title compound was prepared from1-methoxy-4-(6-methyl-2-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-4-yl)cyclohexane-1-carboxylicacid (57 mg, 0.104 mmol) using the same procedured (amide coupling)outlined in Synthetic Protocols 1 and 2, with PyBOP as the amidecoupling reagent instead of HATU. The products were initially isolatedas a mixture of diastereomers (36 mg), which was then dissolved in 6 mLmethanol-DCM (1:1) and purified by SFC (ChiralPak IC-H 21×250 mm, 40%MeOH containing 0.25% DEA in CO₂, 1.0 mL injections, 70 mL/min). Peak 1was an undesired isomer, and Peak 2 was concentrated to give(1s,4R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-1-methoxy-4-(6-methyl-2-((5-methyl-1H-pyrazol-3-yl)amino)pyrimidin-4-yl)cyclohexane-1-carboxamide(13.4 mg, 24%) as a white solid.

Synthesis of Intermediates Example 7. Synthesis of Ketone and BoronateIntermediates A. Methyl 1-methoxy-4-oxocyclohexane-1-carboxylate

The title compound was prepared as described in WO 2014/130810 A1 page86.

B. Ethyl 1-ethoxy-4-oxocyclohexane-1-carboxylate

Step 1: Synthesis of ethyl8-ethoxy-1,4-dioxaspiro[4.5]decane-8-carboxylate

A solution of 1,4-dioxaspiro[4.5]decan-8-one (20.0 g, 128 mmol) in CHBr₃(3234 g, 1280 mmol) was cooled to 0° C. and potassium hydroxide (57.5 g,1024 mmol) in EtOH (300 mL) was added dropwise over 2.5 hrs. Afterstirring the mixture for 23 h, the mixture was concentrated, and theresidue was partitioned between EtOAc and H₂O. The organic layer waswashed with brine, dried over Na₂SO₄, filtered, and concentrated underreduced pressure to give crude product, which was purified by flashcolumn chromatography on silica gel (gradient elution, PE:EA=15:1 to10:1) to obtain the title compound (18.0 g).

Step 2: Synthesis of ethyl 1-ethoxy-4-oxocyclohexane-1-carboxylate

To a solution of ethyl 8-ethoxy-1,4-dioxaspiro[4.5]decane-8-carboxylate(10 g, 43 mmol) in 1,4-dioxane (250 mL) was added aqueous HCl (6 M, 92.5mL), and the mixture was stirred for 23 h at ambient temperature. Themixture was then diluted with WO and extracted with EtOAc. The organiclayers were washed with brine, dried over Na₂SO₄, filtered, andconcentrated under reduced pressure to give a crude residue, which waspurified by flash column chromatography on silica gel (PE:EA=15:1) toobtain the product (8.0 g). ¹H NMR (400 MHz, DMSO) δ 4.20-4.13 (m, 2H),3.43 (q, J=6.9 Hz, 1H), 2.48-2.39 (m, 1H), 2.24-2.12 (m, 2H), 2.10-2.01(m, 1H), 1.22 (t, J=7.1 Hz, 2H), 1.17 (t, J=7.0 Hz, 2H).

C. Ethyl6,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylate

Step 1: Synthesis of ethyl 2,2-dimethyl-4-oxocyclohexane-1-carboxylate

A solution of methylmagnesium bromide (3M, 109.8 mL, 329.4 mmol) wasadded dropwise to a suspension of CuCN (14.75 g, 164.7 mmol) in diethylether (50 mL) at 0° C. The mixture was stirred for 30 min at 0° C. andthen cooled to −78° C. The solution of ethyl2-methyl-4-oxocyclohex-2-ene-1-carboxylate (10 g, 54.9 mmol) in diethylether (10 mL) was then added dropwise. The mixture was stirred between−40° C. to −20° C. for 2 h, then was warmed to ambient temperature for16 h. The reaction mixture was carefully added to a saturated solutionof ammonium chloride. The aqueous layer was extracted twice with diethylether, and the organic layers were combined. The combined organic layerwas washed with brine, dried over sodium sulfate, filtered andconcentrated. The residue was purified by flash column chromatography onsilica gel (PE:EA=10:1) to give ethyl2,2-dimethyl-4-oxocyclohexane-1-carboxylate (1.16 g).

Step 2: Synthesis of ethyl6,6-dimethyl-4-(((trifluoromethyl)sulfonyl)oxy)cyclohex-3-ene-1-carboxylate

Ethyl 2,2-dimethyl-4-oxocyclohexane-1-carboxylate (1.16 g, 5.85 mmol)and DIPEA (3.03 g, 23.4 mmol) were dissolved in dry toluene (2 mL) andheated at 45° C. for 10 minutes. Trifluoromethanesulfonic anhydride(6.61 g, 23.4 mmol) in DCM (20 mL) was added dropwise over 10 min andthe mixture was heated at 45° C. for 2 h. The mixture was allowed tocool to room temperature, concentrated, diluted with water (60 mL) andextracted with DCM (2×40 mL). The organic layer was washed withsaturated sodium bicarbonate solution (20 mL) and brine (20 mL), driedover sodium sulfate, filtered, and concentrated. The crude product waspurified by flash column chromatography on silica gel (gradient elution,0 to 100% ethyl acetate-petroleum ether) to afford ethyl6,6-dimethyl-4-(((trifluoromethyl)sulfonyl)oxy)cyclohex-3-ene-1-carboxylate(1 g).

Step 3: Synthesis of ethyl6,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylate

Ethyl6,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylate(1 g, 3.03 mmol),4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane(1.15 g, 4.54 mmol), Pd(dppf)Cl₂ (73.5 mg, 0.09 mmol) and potassiumacetate (891 mg, 9.08 mmol) were suspended in 1,4-dioxane (20 mL). Thereaction mixture was flushed with nitrogen, then heated to 100° C. for 2h. The mixture was cooled to room temperature, filtered, andconcentrated, and the resulting brown oil was purified by flash columnchromatography on silica gel (gradient elution, 0 to 100% ethylacetate-petroleum ether) to afford ethyl6,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylate(618 mg).

D. Ethyl6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylate

Ethyl6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-ene-1-carboxylatewas prepared using the same synthetic protocol as described above usingethyl 2-methyl-4-oxocyclohexane-1-carboxylate as the starting material.

E. Methyl 2-methyl-5-oxotetrahydro-2H-pyran-2-carboxylate

Step 1: Synthesis of methyl 2-methyl-3,4-dihydro-2H-pyran-2-carboxylate

A mixture of acrylaldehyde (120 g, 2.14 mol), methyl methacrylate (200g, 2.00 mol) and hydroquinone (2.2 g, 20 mmol) were heated in a sealedsteel vessel at 180° C. for one h. The mixture was then cooled toambient temperature and concentrated. The residue was purified by silicagel column chromatography (gradient elution, petroleum ether:ethylacetate=100:1 to 80:1) to give methyl2-methyl-3,4-dihydro-2H-pyran-2-carboxylate (70 g, 22% yield) as a paleyellow oil. ¹H-NMR (400 MHz, CDCl3): δ 6.38 (d, J=6.4 Hz, 1H), 4.73-4.70(m, 1H), 3.76 (s, 3H), 2.25-2.22 (m, 1H), 1.99-1.96 (m, 2H), 1.79-1.77(m, 1H), 1.49 (s, 3H).

Step 2: Synthesis of methyl5-hydroxy-2-methyltetrahydro-2H-pyran-2-carboxylate

To a solution of methyl 2-methyl-3,4-dihydro-2H-pyran-2-carboxylate(20.0 g, 128 mmol) in anhydrous tetrahydrofuran (200 mL) was addedborane (67 mL, 1 M in tetrahydrofuran) dropwise at −5° C. The reactionmixture was stirred at 0° C. for 3 hours. This reaction was monitored byTLC. The mixture was quenched by a solution of sodium acetate (10.5 g,128 mmol) in water (15 mL). Then the mixture was treated with 30%hydrogen peroxide solution (23.6 g, 208.2 mmol) slowly at 0° C. andstirred at 30° C. for 3 h. The mixture was then partitioned betweensaturated sodium sulfite solution and tetrahydrofuran. The aqueous layerwas further extracted with tetrahydrofuran (2×). The combined organiclayers were washed with saturated brine, dried over sodium sulfate andconcentrated in vacuo. The residue was purified by a silica gel columnchromatography (gradient elution, petroleum ether:ethyl acetate=10:1 to1:1) to give crude methyl5-hydroxy-2-methyltetrahydro-2H-pyran-2-carboxylate (18 g, crude) as apale yellow oil, which used directly for next step.

Step 3: Synthesis of methyl2-methyl-5-oxotetrahydro-2H-pyran-2-carboxylate

To a solution of methyl5-hydroxy-2-methyltetrahydro-2H-pyran-2-carboxylate (18.0 g, 103 mmol)in anhydrous dichloromethane (200 mL) was added PCC (45.0 g, 209 mmol)in portions. The reaction mixture was stirred at ambient temperatureuntil TLC indicated the reaction was completed. Petroleum ether (500 mL)was then added and the mixture was filtered. The filter cake was washedwith petroleum ether (100 mL), and the filtrate was concentrated undervacuum to give methyl 2-methyl-5-oxotetrahydro-2H-pyran-2-carboxylate(15 g, 84% yield) as a pale yellow oil. ¹H-NMR (400 MHz, CDCl₃): δ 4.25(d, J=17.6 Hz, 1H), 4.07 (d, J=17.6 Hz, 1H), 3.81 (s, 3H), 2.52-2.44 (m,3H), 2.11-2.04 (m, 1H), 1.53 (s, 3H).

Example 8. Synthesis of Iodide Intermediates A. Methyl1-methoxy-4-iodocyclohexane-1-carboxylate

Step 1: Synthesis of methyl 1-methoxy-4-hydroxycyclohexane-1-carboxylate

Methyl 1-methoxy-4-oxocyclohexanecarboxylate (4.00 g, 21.5 mmol) wasdissolved in methanol (100 mL) and the solution was cooled to 0° C.Sodium borohydride (2.03 g, 53.7 mmol) was added in portions over 20min. The reaction mixture was stirred for 30 min, then was quenched byaddition of aqueous saturated NH₄Cl solution. The quenched reactionmixture was evaporated to remove the MeOH, then the aqueous suspensionwas extracted with DCM (3×). The combined organic layers were dried oversodium sulfate, filtered, and concentrated to yield a residue that waspurified by flash-column chromatography on silica gel (gradient elution,5% to 100% ethyl acetate-hexanes) to afford methyl1-methoxy-4-hydroxycyclohexane-1-carboxylate (2.00 g, 49.5%) as acolorless oil. MS (ES+) C₉H₁₆O₄ requires: 188, found: 211 [M+Na]⁺.

Step 2: Synthesis of methyl 1-methoxy-4-iodocyclohexane-1-carboxylate

Methyl 1-methoxy-4-hydroxycyclohexane-1-carboxylate (2.00 g, 10.6 mmol)was dissolved in THF (20 mL) and imidazole (723 mg, 10.6 mmol) andtriphenylphosphine (3.34 g, 12.8 mmol) were added. The mixture wascooled to 0° C., and then a solution of iodine (3.24 g, 12.8 mmol) inTHF (10 mL) was added dropwise over 15 min. The reaction mixture wasallowed to warm to ambient temperature and was then stirred for 2 days,after which it was poured over saturated sodium thiosulfate solution andextracted with EtOAc. The organic layer was dried over sodium sulfate,filtered, concentrated, and the residue was triturated with hexane (40mL, stir for 20 min). The mixture was filtered, and the filtrate wasevaporated to provide a residue that was purified by flash-columnchromatography on silica gel (gradient elution, 0 to 30% ethylacetate-hexanes) to give the title compound (2.37 g, 75%) as a paleyellow oil. MS (ES+) C₉H₁₅IO₃ requires: 298, found: 299 [M+H]⁺.

B. Ethyl 1-ethoxy-4-iodocyclohexane-1-carboxylate

The title compound was prepared as described above using ethyl1-ethoxy-4-oxocyclohexane-1-carboxylate as a starting material.C₁₁H₁₉IO₃ requires: 326, found: 327 [M+H]⁺.

Example 9. Synthesis of Amine Intermediates A.(S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-amine

Step 1: Synthesis of1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-one

4-Fluoro-1H-pyrazole (4.73 g, 55 mmol) and potassium carbonate (17.27 g,125 mmol) were combined and stirred in N,N-dimethylformamide (41.7 mL)for 10 minutes in an open sealed tube before addition of2-bromo-5-acetylpyridine (10 g, 50 mmol). The reaction tube was sealedand stirred for 20 hours at 100° C. The reaction mixture was then cooledto room temperature and poured into water (˜700 mL). The mixture wassonicated and stirred for 20 minutes, after which a beige solid wasisolated by filtration, washed with small amounts of water, and dried toyield 1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-one (9.81 g,96% yield). MS: M+1=206.0.

Step 2: Synthesis of(R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-2-methylpropane-2-sulfinamide

To a stirred room temperature solution of1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-one (9.806 g, 47.8mmol) in THF (96 mL) was added (R)-(+)-t-Butylsulfinamide (5.79 g, 47.8mmol) followed by titanium (IV) ethoxide (21.8 g, 96 mmol). The solutionwas stirred at 75° C. on an oil bath for 15 hours. The reaction solutionwas cooled to room temperature and then to −78° C. (externaltemperature) before the next step. To the −78° C. solution was addeddropwise over nearly 55 minutes L-Selectride (143 mL of 1N in THF, 143mmol). During addition, some bubbling was observed. The reaction wasthen stirred after the addition was completed for 15 minutes at −78° C.before warming to room temperature. LC-MS of sample taken during removalfrom cold bath showed reaction was completed. The reaction was cooled to−50° C. and quenched slowly with methanol (˜10 mL), then poured intowater (600 mL) and stirred. An off-white precipitate was removed byfiltration, with ethyl acetate used for washes. The filtrate was dilutedwith ethyl acetate (800 mL), the layers were separated, and the organiclayer was dried over sodium sulfate, filtered, and concentrated down.The crude was purified by silica gel chromatography to yield(R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-2-methylpropane-2-sulfinamide(10.5 g, 99% purity, 70.3% yield) as a light yellow solid. MS:M+1=311.1.

Step 3: Synthesis of(S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-amine

A solution of(R)—N—((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-2-methylpropane-2-sulfinamide(10.53 g, 33.9 mmol)) in methanol (79 mmol) and 4N HCl/dioxane (85 mL,339 mmol) was stirred for 2.5 hours, at which point LC-MS showedreaction was complete. The reaction solution was poured into diethylether (300 mL) and a sticky solid was formed. The mixture was treatedwith ethyl acetate (200 mL) and sonicated. The solvents were decanted,and the sticky solid was treated with more ethyl acetate (˜200 mL),sonicated and stirred. The bulk of the sticky solid was converted to asuspension. A light yellow solid was isolated by filtration, washed withsmaller amounts of ethyl acetate, and dried to yield(S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-amine (7.419 g,78% yield). LC-MS confirmed desired product in high purity. MS:M+1=207.1.

B. (S)-1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethan-1-amine

Step 1: Synthesis of1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethan-1-one

Sodium hydride (60 wt %, 276 mg, 6.90 mmol) was added to a mixture of1-(5-chloropyrazin-2-yl)ethanone (800 mg, 5.11 mmol) and4-fluoro-1H-pyrazole (484 mg, 5.62 mmol) in N,N-dimethylformamide (6.0mL) at ambient temperature for 10 minutes. The reaction mixture was thenpoured into water (70 mL) and sonicated and stirred for 20 minutes. Adark red solid was isolated by filtration, washed with small amounts ofwater, and dried to1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethan-1-one (919 mg, 95%yield). MS: M+1=207.

Step 2: Synthesis of(R)—N—((S)-1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethyl)-2-methylpropane-2-sulfinamide

To a stirred room temperature solution of1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethan-1-one (4.67 g, 22.7mmol) in THF (45 mL) was added (R)-(+)-t-butylsulfinamide (2.75 g, 22.7mmol) followed by titanium (IV) ethoxide (10.3 g, 45.3 mmol). Thesolution was stirred at 75° C. on an oil bath for 20 hours. The reactionsolution was cooled to room temperature and then to −78° C. before thenext step. To the −78° C. solution was added dropwise over 50 minutesL-Selectride (50.1 mL of 1 N in THF, 50.1 mmol). During addition, somebubbling was observed. After the addition was completed, the reactionwas then stirred for 15 minutes before warming to room temperature.LC-MS of sample taken during removal from cold bath showed reaction wascompleted. The reaction was cooled to −60° C. and quenched slowly withmethanol (1 mL), then poured into water (100 mL) and stirred. Themixture was filtered and the solids were washed further with ethylacetate. The filtrate was diluted with ethyl acetate, and the organiclayer was dried over sodium sulfate, filtered, concentrated, and theresulting residue was purified by flash-column chromatography (gradientelution, 0 to 100% ethyl acetate-dichloromethane) to give(R)—N—((S)-1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethyl)-2-methylpropane-2-sulfinamide(1.04 g, 14%) as a brown solid. MS: M+1=312. ¹H NMR (400 MHz, DMSO-d6) δ9.12 (d, J=1.4 Hz, 1H), 8.73 (d, J=4.5 Hz, 1H), 8.59 (d, J=1.4 Hz, 1H),8.03 (d, J=4.1 Hz, 1H), 5.69 (d, J=5.7 Hz, 1H), 4.62 (p, J=6.8 Hz, 3H),1.57 (d, J=6.9 Hz, 3H), 1.12 (s, 9H).

Step 3: Synthesis of(S)-1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethan-1-amine

A solution of(R)—N—((S)-1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethyl)-2-methylpropane-2-sulfinamide(1.04 g, 3.34 mmol) in methanol (7.8 mL) and 4N HO/dioxane (8.34 mL,33.4 mmol) was stirred for 1.5 h at ambient temperature. The reactionmixture was poured into diethyl ether (100 mL), and a light beige solidwas isolated by filtration to afford(S)-1-(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)ethan-1-amine (689 mg,85% yield). MS: M+1=208.

C. (5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)methanamine

Step 1: Synthesis of 5-(4-fluoro-1H-pyrazol-1-yl)pyrazine-2-carbonitrile

To a solution of 5-chloropyrazine-2-carbonitrile (280 mg, 2.0 mmol) inDMF was added 4-fluoro-1H-pyrazole (170 mg, 2.0 mmol) and potassiumacetate (395 mg, 4.0 mmol). The mixture was stirred at 100° C. for 4hours, then cooled to 20° C., poured into brine (25 mL), and extractedwith ethyl acetate. The organic layer was dried over sodium sulfate,concentrated, and purified by column chromatography (hexane:ethylacetate=5:1) to give 5-(4-fluoro-1H-pyrazol-1-yl)pyrazine-2-carbonitrile(310 mg, 82%). The structure was confirmed by LC-MS.

Step 2: Synthesis of(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)methanamine

A mixture of 5-(4-fluoro-1H-pyrazol-1-yl)pyrazine-2-carbonitrile (190mg, 1.0 mmol) and NiCl₂ (12 mg, 0.1 mmol) in MeOH (5 mL) was added NaBH₄(380 mg, 10 mmol) at 0° C. The mixture was stirred at 0° C. for 2 hours,quenched with aqueous NH₄Cl, and purified by HPLC to give(5-(4-fluoro-1H-pyrazol-1-yl)pyrazin-2-yl)methanamine (160 mg, Yield82%). The structure was confirmed by LC-MS.

D. (6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridin-3-yl)methanamine

Step 1: Synthesis of 6-(3,5-dimethyl-1H-pyrazol-1-yl)nicotinonitrile

To a solution of 6-chloronicotinonitrile (300 mg, 2.2 mmol) in DMF (10mL) was added 3,5-dimethyl-1H-pyrazole (210 mg, 2.2 mmol) and Cs₂CO₃(1.4 g, 4.4 mmol), and the mixture was stirred at 90° C. for 16 h. Themixture was then diluted with H₂O (25 mL) and filtered. The solids werewashed with water and dried under vacuum to give6-(3,5-Dimethyl-1H-pyrazol-1-yl)nicotinonitrile (320 mg, 74.6%).

Step 2: Synthesis of tert-Butyl((6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridin-3-yl)methyl)carbamate

To 6-(3,5-dimethyl-1H-pyrazol-1-yl)nicotinonitrile (300 mg, 1.5 mmol) inMeOH (10 mL) was added NiCl₂ (19 mg, 0.15 mmol), (Boc)₂O (654 mg, 3.0mmol), and NaBH₄ (142 mg, 3.8 mmol), and the mixture was stirred atambient temperature for 3 h. Saturated aqueous ammonium chloridesolution was added, and MeOH was removed under vacuum. The aqueoussuspension was partitioned with ethyl acetate, and the organic layer waswashed with saturated sodium bicarbonate solution (2×50 mL), dried withanhydrous sodium sulfate, filtered, and concentrated under vacuum togive 450 mg target compound which was used in the next step withoutfurther purification.

Step 3: Synthesis of(6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridin-3-yl)methanamine

A solution of HCl in dioxane (4.0 M, 10 mL) was added to compoundtert-butyl((6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridin-3-yl)methyl)carbamate (450mg), and the mixture was stirred for 2 h. The mixture was thenconcentrated under reduced pressure to give the title compound (350 mg)as a light brown solid that was carried forward without furtherpurification. ¹H NMR (400 MHz, DMSO-d6) δ 8.51 (d, J=2.1 Hz, 1H), 8.34(s, 3H), 8.03 (dd, J=8.5, 2.4 Hz, 1H), 7.87 (d, J=8.5 Hz, 1H), 6.14 (s,1H), 4.12 (q, J=5.7 Hz, 2H), 2.59 (s, 3H), 2.21 (s, 3H).

E. (6-(4-chloro-1H-pyrazol-1-yl)pyridin-3-yl)methanamine

Step 1: Synthesis of 6-(4-Chloro-1H-pyrazol-1-yl)nicotinonitrile

To a solution of 6-chloronicotinonitrile (300 mg, 2.2 mmol) in DMF (10mL) was added 4-chloro-1H-pyrazole (227 mg, 2.2 mmol) and Cs₂CO₃ (1.4 g,4.4 mmol) and the mixture was stirred at 90° C. for 16 h. The mixturewas then diluted with H₂O (25 mL) and filtered. The solids were washedwith H₂O and dried under vacuum to give6-(4-chloro-1H-pyrazol-1-yl)nicotinonitrile (380 mg, 84%), which wasused in the next step without further purification.

Step 2: Synthesis of tert-Butyl((6-(4-chloro-1H-pyrazol-1-yl)pyridin-3-yl)methyl)carbamate

To 6-(4-chloro-1H-pyrazol-1-yl)nicotinonitrile (350 mg, 1.7 mmol) inMeOH (10 mL), was added NiCl₂ (19 mg, 0.17 mmol), (Boc)₂O (741 mg, 3.4mmol) and NaBH₄ (163 mg, 4.3 mmol), and the mixture was stirred atambient temperature for 3 h. Saturated aqueous NH₄Cl solution was added,and the MeOH was removed under vacuum. The aqueous suspension was thenpartitioned with EtOAc, and the organic layer was washed with saturatedsodium bicarbonate solution (2×50 mL), dried with anhydrous sodiumsulfate, filtered, and concentrated under vacuum to give 480 mg of thetitle compound, which was used in the next step without furtherpurification.

Step 3: Synthesis of(6-(4-chloro-1H-pyrazol-1-yl)pyridin-3-yl)methanamine

A solution of HCl in dioxane (4.0 M, 10 mL) was added to tert-butyl((6-(4-chloro-1H-pyrazol-1-yl)pyridin-3-yl)methyl)carbamate (450 mg, 1.5mmol) at ambient temperature. The mixture was stirred for 2 h, thenconcentrated under reduced pressure to give the title compound (290 mg)as a light brown solid that was used without further purification. MS:M+1=209.

F. (R)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-amine

Steps 1-3: (R)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-amine

The title compound was prepared from1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethan-1-one using the samesequence that was described to prepare the S enantiomer of thiscompound, except that (R)-(−)-t-Butylsulfinamide was replaced with(S)-(−)-t-Butylsulfinamide as the chiral auxiliary. MS (ES+) C₁₀H₁₁FN₄requires: 206, found: 207 [M+H]⁺.

The synthetic protocols that can be used to prepare the compoundsdisclosed herein are indicated below. The NMR and LC MS data obtainedfor compounds disclosed herein are also shown below.

Compound Synthetic MS Number Protocol 1H NMR (M + 1) 100 2 ¹H NMR (400MHz, DMSO-d6) δ 472 8.56 (s, 1H), 8.44 (s, 1H), 8.35 (s, 1H), 7.85 (s,2H), 7.81 (s, 1H), 6.66 (d, J = 15.8 Hz, 1H), 6.57 (s, 1H), 4.36 (s,2H), 3.17 (s, 3H), 2.21 (d, J = 29.3 Hz, 3H), 2.06 (d, J = 13.0 Hz, 4H),1.80 (s, 2H), 1.63 (s, 2H). 101 2 ¹H NMR (400 MHz, DMSO) δ 472 8.61 (d,J = 2.5 Hz, 1H), 8.46 (d, J = 6.0 Hz, 1H), 8.36 (s, 1H), 7.91 (d, J =8.4 Hz, 1H), 7.87-7.84 (m, 1H), 7.82 (s, 1H), 6.72-6.66 (m, 1H),6.59-6.57 (m, 1H), 4.34 (d, J = 5.8 Hz, 2H), 3.17 (s, 3H), 2.27 (s, 3H),2.04 (s, 2H), 1.96 (d, J = 11.6 Hz, 2H), 1.59 (dd, J = 27.2, 14.4 Hz,4H). 102 2 1H NMR (400 MHz, DMSO) δ 486 8.56 (s, 1H), 8.44 (s, 1H), 8.35(s, 1H), 7.83 (d, J = 15.0 Hz, 3H), 6.66 (d, J = 15.8 Hz, 1H), 6.57 (s,1H), 4.36 (s, 1H), 3.17 (s, 3H), 2.42 (s, 2H), 2.21 (d, J = 29.3 Hz,3H), 2.06 (d, J = 13.0 Hz, 4H), 1.78 (d, J = 16.2 Hz, 2H), 1.63 (s, 2H).103 2 ¹H NMR (400 MHz, DMSO-d6) δ 486 8.61 (d, J = 2.5 Hz, 1H), 8.46 (d,J = 6.0 Hz, 1H), 8.36 (s, 1H), 7.92- 7.82 (m, 3H), 6.72-6.66 (m, 1H),6.58-6.57 (m, 1H), 4.33 (s, 1H), 3.17 (s, 3H), 2.42 (s, 2H), 2.27 (s,3H), 2.06-1.94 (m, 4H), 1.56 (dd, J = 28.0, 12.9 Hz, 4H). 104 2 ¹H NMR(400 MHz, DMSO-d6) δ 486 14.03 (s, 1H), 12.33 (s, 1H), 8.70- 8.31 (m,4H), 7.86 (d, J = 30.5 Hz, 3H), 6.57 (s, 1H), 4.34 (s, 2H), 2.82 (s,1H), 2.41 (s, 3H), 2.21 (s, 5H), 1.94 (d, J = 12.4 Hz, 1H), 1.67 (dd, J= 45.4, 19.9 Hz, 5H), 1.24 (s, 1H), 0.94 (d, J = 6.4 Hz, 3H). 105 2 ¹HNMR (400 MHz, DMSO-d6) δ 490 8.64 (s, 1H), 8.46 (s, 1H), 8.35 (s, 1H),7.92 (d, J = 4.2 Hz, 1H), 7.86 (d, J = 6.5 Hz, 2H), 6.66 (d, J = 21.2Hz, 1H), 4.36 (s, 2H), 2.91 (s, 1H), 2.42 (s, 2H), 2.21 (d, J = 33.5 Hz,3H), 2.07 (dd, J = 14.5, 7.1 Hz, 4H), 1.80 (s, 2H), 1.64 (d, J = 11.5Hz, 2H). 106 2 ¹H NMR (400 MHz, DMSO-d6) δ 500 11.55 (s, 1H), 11.24 (s,1H), 8.90 (d, J = 5.0 Hz, 1H), 8.44 (s, 1H), 8.33 (s, 1H), 8.01-7.95 (m,0H), 7.81-7.78 (m, 1H), 6.68 (s, 1H), 6.10 (s, 1H), 5.93 (s, 1H), 4.35(s, 2H), 2.91 (s, 0H), 2.54 (s, 1H), 2.44 (d, J = 20.0 Hz, 2H), 2.22 (d,J = 22.8 Hz, 5H), 2.13- 1.96 (m, 4H), 1.79 (d, J = 8.4 Hz, 2H), 1.62 (s,2H). 107 1 ¹H NMR (400 MHz, DMSO-d6) δ 501 14.57 (s, 1H), 12.87 (s, 1H),11.57 (s, 1H), 8.61 (d, J = 2.5 Hz, 1H), 8.47-8.35 (m, 2H), 7.94-7.85(m, 2H), 7.82 (d, J = 1.0 Hz, 1H), 7.11 (s, 1H), 6.95 (s, 1H), 6.58 (dd,J = 2.5, 1.7 Hz, 1H), 6.02 (s, 1H), 5.92 (s, 1H), 4.40-4.29 (m, 2H),2.45 (s, 3H), 2.31 (s, 1H), 2.27 (s, 3H), 2.05-1.96 (m, 2H), 1.93-1.81(m, 3H), 1.54 (d, J = 9.9 Hz, 1H), 0.98 (d, J = 7.2 Hz, 3H). 111 2 ¹HNMR (500 MHz, DMSO-d6) δ 504 11.85 (s, 1H), 9.43 (s, 1H), 8.64 (d, J =4.5 Hz, 1H), 8.35 (d, J = 2.2 Hz, 1H), 8.20 (d, J = 7.7 Hz, 1H),7.92-7.81 (m, 3H), 6.79 (s, 1H), 6.17 (s, 1H), 5.02-4.92 (m, 1H), 2.72(s, 1H), 2.41-2.31 (m, 1H), 2.27-2.12 (m, 8H), 1.83-1.48 (m, 6H), 1.38(d, J = 7.1 Hz, 3H). 506 113 2 ¹H NMR (400 MHz, DMSO-d6) δ 11.55 (s,0H), 11.23 (s, 0H), 8.83 (d, J = 4.8 Hz, 0H), 8.74 (s, 0H), 8.46 (s,0H), 8.36 (s, 0H), 7.95 (s, 0H), 7.90-7.81 (m, 1H), 4.63- 4.48 (m, 0H),4.36 (s, 1H), 2.91 (s, 0H), 2.55 (s, 0H), 2.44 (d, J = 17.9 Hz, 1H),2.20 (d, J = 32.7 Hz, 1H), 2.12-1.85 (m, 1H), 1.62 (s, 1H). 114 1 ¹H NMR(400 MHz, DMSO-d6) δ 515 14.60 (s, 1H), 12.88 (s, 1H), 11.53 (s, 1H),8.61 (m, 1H), 8.36 (dd, J = 12.9, 7.1 Hz, 2H), 7.90 (m, 2H), 7.82 (d, J= 1.0 Hz, 1H), 7.12 (s, 1H), 6.94 (s, 1H), 6.58 (dd, J = 2.5, 1.7 Hz,1H), 6.02 (s, 1H), 5.91 (s, 1H), 4.40 (dd, J = 15.2, 5.9 Hz, 2H), 4.30(m, 2H), 2.45 (s, 3H), 2.27 (s, 3H), 2.17 (d, J = 9.7 Hz, 3H), 1.83 (d,J = 21.1 Hz, 2H), 1.66 (t, J = 16.3 Hz, 2H), 1.13 (s, 3H), 0.94 (s, 3H).116 2 ¹H NMR (400 MHz, DMSO-d6) δ 518 13.88 (s, 1H), 12.46 (s, 1H),11.37 (d, J = 120.9 Hz, 1H), 8.69 (d, J = 4.4 Hz, 1H), 8.50-8.36 (m,2H), 7.98-7.86 (m, 2H), 7.59 (s, 0.5H), 6.86 (d, J = 27.8 Hz, 1H), 6.66(s, 0.5H), 5.91 (s, 0.5H), 5.00 (s, 1H), 2.82 (s, 1H), 2.43 (d, J = 20.6Hz, 3H), 2.22 (s, 3H), 2.11 (s, 1H), 2.04-1.84 (m, 2H), 1.82- 1.57 (m,3H), 1.54 (d, J = 12.6 Hz, 1H), 1.42 (d, J = 5.1 Hz, 3H), 1.24 (s, 1H),1.01 (d, J = 6.8 Hz, 1H), 0.80 (s, 1H) 119 1 ¹H-NMR (400 MHz, DMSO-d6) δ519 ppm 11.63 (s, 1H), 8.85 (s, 1H), 8.65 (d, 1H, J = 4.4 Hz), 8.36 (d,1H, J = 2.0 Hz), 8.25 (d, 1H, J = 7.2 Hz), 7.92-7.83 (m, 3H), 6.79 (s,1H), 6.66 (s, 1H), 6.24 (s, 1H), 5.00 (q, 1H, J = 7.2 Hz), 4.81 (s, 1H),2.49-2.30 (m, 3H), 2.18 (s, 3H), 2.16 (s, 3H), 1.85-1.53 (m, 4H),1.50-1.34 (m, 5H). 124 2 ¹H NMR (400 MHz, DMSO-d6) δ 532 13.84 (s, 1H),12.40 (d, J = 48.8 Hz, 1H), 11.52 (s, 1H), 8.68 (d, J = 3.2 Hz, 1H),8.41 (t, J = 11.2 Hz, 2H), 7.93 (dd, J = 8.4, 2.1 Hz, 2H), 7.89 (dd, J =8.3, 5.2 Hz, 1H), 6.92 (d, J = 24.0 Hz, 1H), 6.65 (s, 1H), 4.98 (s, 1H),3.00 (s, 1H), 2.40 (s, 6H), 2.22 (s, 1H), 2.12 (s, 2H), 1.85 (s, 2H),1.67 (d, J = 15.1 Hz, 2H), 1.42 (d, J = 5.7 Hz, 3H), 1.31 (m, 2H), 1.04(m, 6H). 128 1 ¹H NMR (400 MHz, DMSO-d6) δ 534 14.54 (s, 1H), 12.87 (s,1H), 11.61 (s, 1H), 8.68 (d, J = 4.5 Hz, 1H), 8.41 (dd, J = 6.4, 2.0 Hz,1H), 8.31 (dd, J = 28.8, 7.8 Hz, 1H), 7.97- 7.86 (m, 3H), 7.09 (s, 1H),6.96 (s, 1H), 5.92 (d, J = 3.7 Hz, 1H), 5.04 (d, J = 7.3 Hz, 1H), 2.46(s, 3H), 2.32 (s, 1H), 2.27 (d, J = 5.1 Hz, 3H), 2.12-1.77 (m, 6H), 1.49(d, J = 10.0 Hz, 1H), 1.42 (d, J = 7.0 Hz, 3H), 1.03 (s, 1H), 0.84 (d, J= 7.2 Hz, 2H). 129 3 ¹H NMR (400 MHz, DMSO-d6) δ 534 11.85 (s, 1H), 9.46(s, 1H), 8.65 (d, J = 4.5 Hz, 1H), 8.48-8.35 (m, 2H), 7.96 (dd, J = 8.5,2.3 Hz, 1H), 7.89 (d, J = 4.2 Hz, 1H), 7.84 (d, J = 8.5 Hz, 1H), 6.77(s, 1H), 6.15 (s, 1H), 5.12-5.02 (m, 1H), 3.06 (s, 3H), 2.67 (t, J = 6.4Hz, 1H), 2.20 (s, 3H), 2.16 (s, 5H), 1.95 (dd, J = 28.8, 9.8 Hz, 2H),1.87-1.76 (m, 2H), 1.58-1.38 (m, 5H). 130 3 ¹H NMR (500 MHz, DMSO-d6) δ534 11.89 (s, 1H), 9.51 (bs, 1H), 8.68 (dd, J = 4.5, 0.7 Hz, 1H), 8.46(d, J = 8.5 Hz, 1H), 8.44 (d, J = 2.3 Hz, 1H), 7.99 (dd, J = 8.5, 2.3Hz, 1H), 7.91 (dd, J = 4.4, 0.8 Hz, 1H), 7.88 (d, J = 8.6 Hz, 1H), 6.86(bs, 1H), 6.20 (bs, 1H), 5.06 (dq, J = 7.8, 7.6 Hz 1H), 3.14 (s, 3H),2.58 (bt, J = 12 Hz, 1H), 2.24 (s, 3H), 2.21 (s, 3H), 1.99 (bd, J = 12.1Hz, 1H), 1.93 (dd, J = 13.8, 2.4 Hz, 1H), 1.88-1.69 (m, 5H), 1.63 (td, J= 14, 4 Hz, 1H), 1.47 (d, J = 7.1 Hz, 3H). 131 3 ¹H NMR (400 MHz,DMSO-d6) δ 535 11.88 (s, 1H), 9.51 (s, 1H), 9.12 (d, J = 1.4 Hz, 1H),8.73 (d, J = 4.4 Hz, 1H), 8.51 (d, J = 1.4 Hz, 1H), 8.41 (d, J = 8.0 Hz,1H), 8.02 (d, J = 4.1 Hz, 1H), 6.85 (s, 1H), 6.18 (s, 1H), 5.18-5.07 (m,1H), 3.17 (s, 3H), 2.64-2.52 (m, 1H), 2.23 (s, 3H), 2.19 (s, 3H),2.02-1.91 (m, 2H), 1.89-1.61 (m, 6H), 1.49 (d, J = 7.1 Hz, 3H). 135 1 ¹HNMR (400 MHz, DMSO-d6) δ 547 (14.58 (m, 1H), 12.89 (m, 2H), 11.52 (s,1H), 8.69 (t, J = 4.3 Hz, 1H), 8.43 (d, J = 2.0 Hz, 1H), 8.27 (m, 1H),7.97 (m, 4H), 7.59 (m, 1H), 7.06 (s, 1H), 6.95 (s, 1H), 5.98 (s, 1H),5.91 (s, 1H), 5.06 (dd, J = 13.5, 7.0 Hz, 1H), 2.46 (s, 3H), 2.27 (s,3H), 2.17 (s, 2H), 1.83 (d, J = 29.4 Hz, 2H), 1.62 (s, 2H), 1.52 (d, J =7.0 Hz, 1H), 1.44 (d, J = 7.1 Hz, 3H), 1.16 (s, 1H), 1.04 (s, 2H), 1.02(s, 1H), 0.88 (s, 2H). 136 3 ¹H NMR (400 MHz, DMSO-d6) δ 548 11.89 (s,1H), 9.53 (s, 1H), 8.67 (d, J = 4.4 Hz, 1H), 8.41 (d, J = 2.2 Hz, 1H),8.28 (d, J = 8.2 Hz, 1H), 7.98 (dd, J = 8.5, 2.3 Hz, 1H), 7.93-7.80 (m,2H), 6.74 (s, 1H), 6.28 (s, 1H), 5.09-4.95 (m, 1H), 3.28-3.20 (m, 2H),2.61-2.51 (m, 1H), 2.22 (s, 3H), 2.19 (s, 3H), 2.02-1.91 (m, 2H),1.90-1.78 (m, 2H), 1.71 (d, J = 10.4 Hz, 3H), 1.63-1.51 (m, 1H), 1.45(d, J = 7.1 Hz, 3H), 1.21 (t, J = 6.9 Hz, 3H). 137 1 ¹H NMR (400 MHz,DMSO-d6) δ 549 11.71 (s, 1H), 8.91 (s, 1H), 8.64 (d, J = 4.5 Hz, 1H),8.48-8.36 (m, 2H), 7.97 (dd, J = 8.5, 2.3 Hz, 1H), 7.89 (d, J = 4.2 Hz,1H), 7.83 (d, J = 8.5 Hz, 1H), 6.70 (s, 1H), 6.68 (s, 1H), 6.17 (s, 1H),5.17- 5.08 (m, , 1H), 4.88 (s, 1H), 3.08 (s, 3H), 2.25-2.15 (m, 7H),2.02- 1.73 (m, 6H), 1.59-1.48 (m, 2H), 1.45 (d, J = 7.0 Hz, 3H). 138 1¹H NMR (400 MHz, DMSO-d6) δ 549 11.67 (s, 1H), 8.96 (s, 1H), 8.68 (d, J= 4.5 Hz, 1H), 8.48 (d, J = 8.3 Hz, 1H), 8.43 (d, J = 2.2 Hz, 1H), 7.99(dd, J = 8.6, 2.3 Hz, 1H), 7.94-7.81 (m, 2H), 6.77 (s, 1H), 6.67 (s,1H), 6.39 (s, 1H), 5.09- 5.01 (m, 1H), 4.84 (s, 1H), 3.18 (s, 3H),2.29-2.03 (m, 9H), 1.97 (td, J = 13.7, 3.5 Hz, 1H), 1.72 (dd, J = 20.5,14.9 Hz, 2H), 1.46 (d, J = 7.0 Hz, 3H), 1.40-1.26 (m, 2H). 141 1 ¹H NMR(400 MHz, DMSO-d6) δ 551 11.64 (s, 1H), 9.01 (s, 1H), 8.64 (d, J = 4.5Hz, 1H), 8.55 (d, J = 8.3 Hz, 1H), 8.40 (d, J = 2.3 Hz, 1H), 7.97 (dd, J= 8.5, 2.4 Hz, 1H), 7.89 (d, J = 4.2 Hz, 1H), 7.84 (d, J = 8.5 Hz, 1H),6.78 (s, 1H), 6.66 (s, 1H), 6.27 (s, 1H), 5.14 (t, J = 7.5 Hz, 1H), 3.10(s, 3H), 2.45-2.29 (m, 2H), 2.20 (s, 3H), 2.16 (s, 3H), 2.14-2.01 (m,2H), 1.91-1.68 (m, 4H), 1.46 (d, J = 7.1 Hz, 3H). 142 1 ¹H NMR (400 MHz,DMSO-d6) δ 551 11.71 (s, 1H), 9.11 (s, 1H), 8.67 (d, J = 4.5 Hz, 1H),8.56 (d, J = 8.3 Hz, 1H), 8.43 (d, J = 2.2 Hz, 1H), 7.99 (dd, J = 8.5,2.3 Hz, 1H), 7.93-7.84 (m, 2H), 6.77 (s, 1H), 6.63 (s, 1H), 6.32 (s,1H), 5.10- 05.13 (m, 1H), 3.20 (s, 3H), 2.43- 2.15 (m, 8H), 2.06-1.81(m, 4H), 1.78-1.61 (m, 2H), 1.47 (d, J = 7.1 Hz, 3H). 144 2 ¹H NMR (500MHz, DMSO-d6) δ 502 11.89 (s, 1H), 9.48 (s, 1H), 8.67 (d, J = 4.5 Hz,1H), 8.49-8.30 (m, 2H), 7.96-7.77 (m, 3H), 7.09 (d, J = 7.4, 1H), 6.81(s, 1H), 6.19 (s, 1H), 5.01 (q, J = 7.0 Hz, 1H), 3.16 (d, J = 4.9 Hz,1H), 2.75 (t, J = 18.9 Hz, 1H), 2.41-2.28 (m, 2H), 2.25 (d, J = 1.9 Hz,3H), 2.20 (s, 3H), 2.10-1.87 (m, 1H), 1.65- 1.49 (m, 2H), 1.41 (dd, J =7.0, 2.0 Hz, 3H). 146 1 ¹H NMR (400 MHz, DMSO-d6) δ 521 11.68 (s, 1H),8.91 (s, 1H), 8.69 (d, J = 4.4 Hz, 1H), 8.44 (d, J = 2.3 Hz, 1H), 8.18(d, J = 8.2 Hz, 1H), 7.99 (dd, J = 8.6, 2.4 Hz, 1H), 7.93-7.87 (m, 2H),6.90 (s, 1H), 6.84 (s, 1H), 6.12 (s, 1H), 5.22 (s, 1H), 5.08 (dt, J =14.5, 7.2 Hz, 1H), 3.93-3.81 (m, 2H), 3.72-3.63 (m, 1H), 2.30-2.23 (m,1H), 2.21 (s, 3H), 2.19 (s, 3H), 1.84-1.74 (m, 2H), 1.74-1.65 (m, 1H),1.47 (d, J = 7.0 Hz, 3H). 147 1 ¹H-NMR (400 MHz, CD₃OD): δ 535 ppm8.53-8.51 (m, 2H), 8.43 (d, J = 7.6 Hz, 1H), 8.04-8.02 (m, 1H), 7.95 (d,J = 8.8 Hz, 1H), 7.71 (d, J = 4.0 Hz, 1H), 7.01 (s, 1H), 6.72 (s, 1H),5.91 (s, 1H), 5.18-5.15 (m, 1H), 4.19 (d, J = 11.6 Hz, 1H), 3.60 (d, J =12.0 Hz, 1H), 2.38 (s, 3H), 2.38-2.29 (m, 1H), 2.29 (s, 3H), 2.18-2.13(m, 1H), 1.81- 1.78 (m, 1H), 1.59 (d, J = 7.2 Hz, 3H), 1.59-1.51 (m,1H), 1.51 (s, 3H). 148 1 ¹H-NMR (400 MHz, CD₃OD): δ 535 ppm 8.52 (d, J =4.4 Hz, 1H), 8.47 (d, J = 9.2 Hz, 1H), 7.99-7.93 (m, 2H), 7.71 (d, J =4.0 Hz, 1H), 7.08 (s, 1H), 6.76 (s, 1H), 5.88 (s, 1H), 5.19-5.16 (m,1H), 4.21 (d, J = 12.0 Hz, 1H), 3.70 (d, J = 12.0 Hz, 1H), 2.41 (s, 3H),2.41-2.30 (m, 1H), 2.30 (s, 3H), 2.30-2.22 (m, 1H), 1.92-1.87 (m, 1H),1.64 (d, J = 7.2 Hz, 3H), 1.63-1.46 (m, 1H), 1.46 (s, 3H). 149 4 ¹H NMR(500 MHz, DMSO-d6) δ 534 11.74 (s, 1H), 9.13 (s, 1H), 8.67 (d, J = 4.4Hz, 1H), 8.47 (d, J = 8.3 Hz, 1H), 8.42 (d, J = 2.3 Hz, 1H), 7.98 (dd, J= 8.5, 2.3 Hz, 1H), 7.90 (d, J = 4.2 Hz, 1H), 7.86 (d, J = 8.5 Hz, 1H),6.51 (s, 1H), 6.50 (s, 1H), 5.04 (p, J = 7.6 Hz, 1H), 3.13 (s, 3H), 2.27(s, 3H), 2.19 (s, 3H), 1.95 (dd, J = 29.5, 11.6 Hz, 2H), 1.84-1.54 (m,7H), 1.45 (d, J = 7.1 Hz, 3H). 150 3 ¹H NMR (400 MHz, DMSO) δ 521 11.88(s, 1H), 9.50 (s, 1H), 9.11 (d, J = 1.4 Hz, 1H), 8.72 (d, J = 4.4 Hz,1H), 8.64 (t, J = 6.0 Hz, 1H), 8.39 (d, J = 1.4 Hz, 1H), 8.02 (d, J =4.2 Hz, 1H), 6.85 (s, 1H), 6.17 (s, 1H), 4.48 (d, J = 5.9 Hz, 2H), 3.19(s, 3H), 2.64-2.53 (m, 1H), 2.23 (s, 3H), 2.19 (s, 3H), 1.96 (d, J =14.2 Hz, 2H), 1.86- 1.67 (m, 6H). 151 3 ¹H NMR (400 MHz, DMSO) δ 53411.88 (s, 1H), 9.50 (s, 1H), 8.66 (d, J = 4.4 Hz, 1H), 8.46 (d, J = 8.3Hz, 1H), 8.41 (d, J = 2.2 Hz, 1H), 7.98 (dd, J = 8.5, 2.3 Hz, 1H),7.92-7.82 (m, 2H), 6.84 (s, 1H), 6.18 (s, 1H), 5.08-5.01 (m, 1H), 3.12(s, 3H), 2.61-2.51 (m, 1H), 2.22 (s, 3H), 2.19 (s, 3H), 2.00- 1.87 (m,2H), 1.83-1.56 (m, 6H), 1.45 (d, J = 7.1 Hz, 3H).

Example 10: Measurement of Biochemical Activity of Compounds

In order to assess the activity of chemical compounds against therelevant kinase of interest, the Caliper LifeSciences electrophoreticmobility shift technology platform was used. Fluorescently labeledsubstrate peptide was incubated in the presence of kinase and ATP sothat a reflective proportion of the peptide was phosphorylated. At theend of the reaction, the mix of phosphorylated (product) andnon-phosphorylated (substrate) peptides were passed through themicrofluidic system of the Caliper EZ Reader 2, under an appliedpotential difference. The presence of the phosphate group on the productpeptide provides a difference in mass and charge between those of thesubstrate peptide, resulting in a separation of the substrate andproduct pools in the sample. As the pools pass a LEDS within theinstrument, these pools are detected and resolved as separate peaks. Theratio between these peaks therefore reflects the activity of thechemical matter at that concentration in that well, under thoseconditions.

A. RET Wild Type Assay at KM

In each well of a 384-well plate, 7.5 nM-10 nM of wild type RET(ProQinase 1090-0000-1) was incubated in a total of 12.5 μL of buffer(100 mM HEPES pH 7.5, 0.015% BriJ 35, 10 mM MgCl₂, 1 mM DTT) with 1 μMCSKtide (FITC-AHA-KKKKD DIYFFFG-NH2) and 25 μM ATP at 25° C. for 120minutes in the presence or absence of a dosed concentration series ofcompound (1% DMSO final concentration). The reaction was stopped by theaddition of 70 μL of Stop buffer (100 mM HEPES pH 7.5, 0.015% Brij 35,35 mM EDTA and 0.2% of Coating Reagent 3 (Caliper Lifesciences)). Theplate was then read on a Caliper EZReader 2 (protocol settings: −1.7psi, upstream voltage −500, downstream voltage −3000, post sample sip35s). Data was normalized to 0% and 100% inhibition controls and theIC₅₀ calculated using a 4-parameter fit in the CORE LIMS.

B. RET V804L Gatekeeper Mutant Assay at KM

In each well of a 384-well plate, 7.5 nM-10 nM of mutant RET (ProQinase1096-0000-1) was incubated in a total of 12.5 μL of buffer (100 mM HEPESpH 7.5, 0.015% BriJ 35, 10 mM MgCl2, 1 mM DTT) with 1 μM CSKtide(FITC-AHA-KKKKDDIYFFFG-NH2) and 10 μM ATP at 25° C. for 120 minutes inthe presence or absence of a dosed concentration series of compound (1%DMSO final concentration). The reaction was stopped by the addition of70 μL of Stop buffer (100 mM HEPES pH 7.5, 0.015% Brij 35, 35 mM EDTAand 0.2% of Coating Reagent 3 (Caliper Lifesciences)). The plate wasthen read on a Caliper EZReader 2 (protocol settings: −1.7 psi, upstreamvoltage −500, downstream voltage −3000, post sample sip 35s). Data wasnormalized to 0% and 100% inhibition controls and the IC₅₀ calculatedusing a 4-parameter fit in the CORE LIMS.

In the Table below, the following designations are used: <10.00 nM=A;10.01-100.0 nM=B; and >100 nM=C.

Compound Wild-type V804L Number RET Mutant 100 C C 101 A A 102 C C 103 AA 104 C C 105 B B 106 A B 107 A A 109 A A 110 B B 111 B A 112 A A 113 AA 114 A A 116 C B 119 C C 120 A A 121 A A 122 B B 124 C B 128 A A 129 CC 130 A A 131 A A 135 B B 136 A A 137 C C 138 A A 141 B B 142 A A 144 AA 146 A A 147 B B 148 A A 149 B B 150 A A 151 A A

INCORPORATION BY REFERENCE

All publications and patents mentioned herein are hereby incorporated byreference in their entirety as if each individual publication or patentwas specifically and individually indicated to be incorporated byreference.

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain usingno more than routine experimentation, many equivalents to the specificembodiments of the invention described herein. Such equivalents areintended to be encompassed by the following claims.

1-19. (canceled)
 20. A compound which is:


21. A compound which is:


22. A compound which is:


23. A compound which is: